Canonical Allele Identifier: CA304445642
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs541904990
gnomAD v3: 19-4090482-G-A
gnomAD v4: 19-4090482-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090482G>A , CM000681.2:g.4090482G>A GRCh38
NC_000019.9:g.4090480G>A , CM000681.1:g.4090480G>A GRCh37
NC_000019.8:g.4041480G>A NCBI36
NG_007996.1:g.38647C>T , LRG_750:g.38647C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1758C>T
ENST00000688002.1:n.3470C>T
ENST00000688751.1:n.455C>T
ENST00000689792.1:n.1223C>T
ENST00000262948.10:c.*116C>T MANE Select ENSP00000262948.4:n.*116C>T
ENST00000262948.9:c.*116C>T ENSP00000262948.3:n.*116C>T
ENST00000394867.8:c.*116C>T ENSP00000378336.1:n.*116C>T
ENST00000597263.5:n.504C>T
ENST00000600584.5:n.2768C>T
ENST00000601786.5:n.1620C>T
NM_030662.3:c.*116C>T , LRG_750t1:c.*116C>T NP_109587.1:n.*116C>T
XM_006722799.2:c.*116C>T XP_006722862.1:n.*116C>T
XM_011528133.1:c.*116C>T XP_011526435.1:n.*116C>T
NM_030662.4:c.*116C>T MANE Select NP_109587.1:n.*116C>T