Canonical Allele Identifier: CA403392470

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145079874
• gnomAD v4: 19-4117456-A-G
• MyVariant Identifiers: chr19:g.4117454A>G (hg19) ; chr19:g.4117456A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117456A>G , CM000681.2:g.4117456A>G	GRCh38
NC_000019.9:g.4117454A>G , CM000681.1:g.4117454A>G	GRCh37
NC_000019.8:g.4068454A>G	NCBI36
NG_007996.1:g.11673T>C , LRG_750:g.11673T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.705T>C
ENST00000687128.1:n.705T>C
ENST00000262948.10:c.266T>C MANE Select	ENSP00000262948.4:p.Val89Ala
ENST00000262948.9:c.266T>C	ENSP00000262948.3:p.Val89Ala
ENST00000394867.8:c.-26T>C	ENSP00000378336.1:n.-26T>C
ENST00000599345.1:n.463T>C
NM_030662.3:c.266T>C , LRG_750t1:c.266T>C	NP_109587.1:p.Val89Ala
XM_006722799.2:c.266T>C	XP_006722862.1:p.Val89Ala
XM_017026989.1:c.266T>C	XP_016882478.1:p.Val89Ala
XM_017026990.1:c.266T>C	XP_016882479.1:p.Val89Ala
XM_017026991.1:c.266T>C	XP_016882480.1:p.Val89Ala
NM_030662.4:c.266T>C MANE Select	NP_109587.1:p.Val89Ala