Canonical Allele Identifier: CA659837703
Gene: SHOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1424299410

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964218C>G , CM000672.2:g.110964218C>G GRCh38
NC_000010.10:g.112723976C>G , CM000672.1:g.112723976C>G GRCh37
NC_000010.9:g.112713966C>G NCBI36
NG_028922.1:g.49676C>G , LRG_753:g.49676C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265277.10:c.-141C>G ENSP00000265277.5:n.-141C>G
ENST00000451838.2:c.-242-36197C>G ENSP00000408275.2:n.-242-36197C>G
ENST00000480155.2:n.96C>G
ENST00000685059.1:c.-141C>G ENSP00000510210.1:n.-141C>G
ENST00000685613.1:c.-141C>G ENSP00000510564.1:n.-141C>G
ENST00000687592.1:n.159C>G
ENST00000688928.1:c.-141C>G ENSP00000509273.1:n.-141C>G
ENST00000689118.1:c.-141C>G ENSP00000510554.1:n.-141C>G
ENST00000689300.1:c.-141C>G ENSP00000510639.1:n.-141C>G
ENST00000689997.1:c.-380-21410C>G ENSP00000510700.1:n.-380-21410C>G
ENST00000691151.1:n.152C>G
ENST00000691369.1:c.-141C>G ENSP00000509754.1:n.-141C>G
ENST00000691441.1:c.-141C>G ENSP00000509686.1:n.-141C>G
ENST00000691903.1:c.-141C>G ENSP00000510314.1:n.-141C>G
ENST00000692776.1:c.-141C>G ENSP00000508524.1:n.-141C>G
ENST00000369452.9:c.-141C>G MANE Select ENSP00000358464.5:n.-141C>G
ENST00000265277.9:c.-141C>G ENSP00000265277.5:n.-141C>G
ENST00000369452.8:c.-141C>G ENSP00000358464.4:n.-141C>G
ENST00000480155.1:n.344C>G
ENST00000489390.1:n.56-36197C>G
ENST00000489783.1:n.238C>G
NM_001269039.1:c.-141C>G NP_001255968.1:n.-141C>G
NM_007373.3:c.-141C>G , LRG_753t1:c.-141C>G NP_031399.2:n.-141C>G
XM_011540216.1:c.-380-21410C>G XP_011538518.1:n.-380-21410C>G
NM_001269039.2:c.-141C>G NP_001255968.1:n.-141C>G
NM_001324336.1:c.-141C>G NP_001311265.1:n.-141C>G
NM_001324337.1:c.-141C>G NP_001311266.1:n.-141C>G
NR_136749.1:n.116-21410C>G
NM_007373.4:c.-141C>G MANE Select NP_031399.2:n.-141C>G
NM_001269039.3:c.-141C>G NP_001255968.1:n.-141C>G
NM_001324336.2:c.-141C>G NP_001311265.1:n.-141C>G
NM_001324337.2:c.-141C>G NP_001311266.1:n.-141C>G
NR_136749.2:n.55-21410C>G