Canonical Allele Identifier: CA882241169
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1365384657
gnomAD v3: 19-4090426-G-A
gnomAD v4: 19-4090426-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090426G>A , CM000681.2:g.4090426G>A GRCh38
NC_000019.9:g.4090424G>A , CM000681.1:g.4090424G>A GRCh37
NC_000019.8:g.4041424G>A NCBI36
NG_007996.1:g.38703C>T , LRG_750:g.38703C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1814C>T
ENST00000688751.1:n.511C>T
ENST00000689792.1:n.1279C>T
ENST00000262948.10:c.*172C>T MANE Select ENSP00000262948.4:n.*172C>T
ENST00000262948.9:c.*172C>T ENSP00000262948.3:n.*172C>T
ENST00000394867.8:c.*172C>T ENSP00000378336.1:n.*172C>T
ENST00000600584.5:n.2824C>T
ENST00000601786.5:n.1676C>T
NM_030662.3:c.*172C>T , LRG_750t1:c.*172C>T NP_109587.1:n.*172C>T
XM_006722799.2:c.*172C>T XP_006722862.1:n.*172C>T
XM_011528133.1:c.*172C>T XP_011526435.1:n.*172C>T
NM_030662.4:c.*172C>T MANE Select NP_109587.1:n.*172C>T