Canonical Allele Identifier: CA2319219660
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs2040844197
gnomAD v4: 19-4090474-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090474T>C , CM000681.2:g.4090474T>C GRCh38
NC_000019.9:g.4090472T>C , CM000681.1:g.4090472T>C GRCh37
NC_000019.8:g.4041472T>C NCBI36
NG_007996.1:g.38655A>G , LRG_750:g.38655A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1766A>G
ENST00000688002.1:n.3478A>G
ENST00000688751.1:n.463A>G
ENST00000689792.1:n.1231A>G
ENST00000262948.10:c.*124A>G MANE Select ENSP00000262948.4:n.*124A>G
ENST00000262948.9:c.*124A>G ENSP00000262948.3:n.*124A>G
ENST00000394867.8:c.*124A>G ENSP00000378336.1:n.*124A>G
ENST00000597263.5:n.512A>G
ENST00000600584.5:n.2776A>G
ENST00000601786.5:n.1628A>G
NM_030662.3:c.*124A>G , LRG_750t1:c.*124A>G NP_109587.1:n.*124A>G
XM_006722799.2:c.*124A>G XP_006722862.1:n.*124A>G
XM_011528133.1:c.*124A>G XP_011526435.1:n.*124A>G
NM_030662.4:c.*124A>G MANE Select NP_109587.1:n.*124A>G