Canonical Allele Identifier: CA304445573
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs781375177
gnomAD v2: 19-4090409-C-A
gnomAD v3: 19-4090411-C-A
gnomAD v4: 19-4090411-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090411C>A , CM000681.2:g.4090411C>A GRCh38
NC_000019.9:g.4090409C>A , CM000681.1:g.4090409C>A GRCh37
NC_000019.8:g.4041409C>A NCBI36
NG_007996.1:g.38718G>T , LRG_750:g.38718G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1829G>T
ENST00000688751.1:n.526G>T
ENST00000689792.1:n.1294G>T
ENST00000262948.10:c.*187G>T MANE Select ENSP00000262948.4:n.*187G>T
ENST00000262948.9:c.*187G>T ENSP00000262948.3:n.*187G>T
ENST00000394867.8:c.*187G>T ENSP00000378336.1:n.*187G>T
ENST00000600584.5:n.2839G>T
ENST00000601786.5:n.1691G>T
NM_030662.3:c.*187G>T , LRG_750t1:c.*187G>T NP_109587.1:n.*187G>T
XM_006722799.2:c.*187G>T XP_006722862.1:n.*187G>T
XM_011528133.1:c.*187G>T XP_011526435.1:n.*187G>T
NM_030662.4:c.*187G>T MANE Select NP_109587.1:n.*187G>T