Canonical Allele Identifier: CA403392488

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2041237567
• gnomAD v4: 19-4117465-A-C
• MyVariant Identifiers: chr19:g.4117463A>C (hg19) ; chr19:g.4117465A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117465A>C , CM000681.2:g.4117465A>C	GRCh38
NC_000019.9:g.4117463A>C , CM000681.1:g.4117463A>C	GRCh37
NC_000019.8:g.4068463A>C	NCBI36
NG_007996.1:g.11664T>G , LRG_750:g.11664T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.696T>G
ENST00000687128.1:n.696T>G
ENST00000262948.10:c.257T>G MANE Select	ENSP00000262948.4:p.Val86Gly
ENST00000262948.9:c.257T>G	ENSP00000262948.3:p.Val86Gly
ENST00000394867.8:c.-35T>G	ENSP00000378336.1:n.-35T>G
ENST00000599345.1:n.454T>G
NM_030662.3:c.257T>G , LRG_750t1:c.257T>G	NP_109587.1:p.Val86Gly
XM_006722799.2:c.257T>G	XP_006722862.1:p.Val86Gly
XM_017026989.1:c.257T>G	XP_016882478.1:p.Val86Gly
XM_017026990.1:c.257T>G	XP_016882479.1:p.Val86Gly
XM_017026991.1:c.257T>G	XP_016882480.1:p.Val86Gly
NM_030662.4:c.257T>G MANE Select	NP_109587.1:p.Val86Gly