Canonical Allele Identifier: CA631537015

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1449764381
• gnomAD v2: 19-4090556-T-C
• gnomAD v4: 19-4090558-T-C
• MyVariant Identifiers: chr19:g.4090556T>C (hg19) ; chr19:g.4090558T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090558T>C , CM000681.2:g.4090558T>C	GRCh38
NC_000019.9:g.4090556T>C , CM000681.1:g.4090556T>C	GRCh37
NC_000019.8:g.4041556T>C	NCBI36
NG_007996.1:g.38571A>G , LRG_750:g.38571A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1682A>G
ENST00000688002.1:n.3394A>G
ENST00000688751.1:n.379A>G
ENST00000689792.1:n.1147A>G
ENST00000262948.10:c.*40A>G MANE Select	ENSP00000262948.4:n.*40A>G
ENST00000262948.9:c.*40A>G	ENSP00000262948.3:n.*40A>G
ENST00000394867.8:c.*40A>G	ENSP00000378336.1:n.*40A>G
ENST00000597263.5:n.428A>G
ENST00000600584.5:n.2692A>G
ENST00000601786.5:n.1544A>G
NM_030662.3:c.*40A>G , LRG_750t1:c.*40A>G	NP_109587.1:n.*40A>G
XM_006722799.2:c.*40A>G	XP_006722862.1:n.*40A>G
XM_011528133.1:c.*40A>G	XP_011526435.1:n.*40A>G
NM_030662.4:c.*40A>G MANE Select	NP_109587.1:n.*40A>G