Canonical Allele Identifier: CA403380672
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs117945277
gnomAD v2: 19-4090612-G-C
gnomAD v4: 19-4090614-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090614G>C , CM000681.2:g.4090614G>C GRCh38
NC_000019.9:g.4090612G>C , CM000681.1:g.4090612G>C GRCh37
NC_000019.8:g.4041612G>C NCBI36
NG_007996.1:g.38515C>G , LRG_750:g.38515C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1626C>G
ENST00000688002.1:n.3338C>G
ENST00000688751.1:n.323C>G
ENST00000689792.1:n.1091C>G
ENST00000262948.10:c.1187C>G MANE Select ENSP00000262948.4:p.Thr396Arg
ENST00000262948.9:c.1187C>G ENSP00000262948.3:p.Thr396Arg
ENST00000394867.8:c.896C>G ENSP00000378336.1:p.Thr299Arg
ENST00000597263.5:n.372C>G
ENST00000599021.1:c.297C>G
ENST00000600584.5:n.2636C>G
ENST00000601786.5:n.1488C>G
NM_030662.3:c.1187C>G , LRG_750t1:c.1187C>G NP_109587.1:p.Thr396Arg
XM_006722799.2:c.908C>G XP_006722862.1:p.Thr303Arg
XM_011528133.1:c.617C>G XP_011526435.1:p.Thr206Arg
NM_030662.4:c.1187C>G MANE Select NP_109587.1:p.Thr396Arg