Canonical Allele Identifier: CA2319219583
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs2040843020
gnomAD v4: 19-4090374-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090374A>C , CM000681.2:g.4090374A>C GRCh38
NC_000019.9:g.4090372A>C , CM000681.1:g.4090372A>C GRCh37
NC_000019.8:g.4041372A>C NCBI36
NG_007996.1:g.38755T>G , LRG_750:g.38755T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1866T>G
ENST00000688751.1:n.563T>G
ENST00000689792.1:n.1331T>G
ENST00000262948.10:c.*224T>G MANE Select ENSP00000262948.4:n.*224T>G
ENST00000262948.9:c.*224T>G ENSP00000262948.3:n.*224T>G
ENST00000394867.8:c.*224T>G ENSP00000378336.1:n.*224T>G
ENST00000600584.5:n.2876T>G
ENST00000601786.5:n.1728T>G
NM_030662.3:c.*224T>G , LRG_750t1:c.*224T>G NP_109587.1:n.*224T>G
XM_006722799.2:c.*224T>G XP_006722862.1:n.*224T>G
XM_011528133.1:c.*224T>G XP_011526435.1:n.*224T>G
NM_030662.4:c.*224T>G MANE Select NP_109587.1:n.*224T>G