Canonical Allele Identifier: CA2735392355

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2040962847

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099161A>G , CM000681.2:g.4099161A>G	GRCh38
NC_000019.9:g.4099159A>G , CM000681.1:g.4099159A>G	GRCh37
NC_000019.8:g.4050159A>G	NCBI36
NG_007996.1:g.29968T>C , LRG_750:g.29968T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+40T>C
ENST00000687128.1:n.1398T>C
ENST00000688002.1:n.1253T>C
ENST00000689792.1:n.823+40T>C
ENST00000262948.10:c.919+40T>C MANE Select	ENSP00000262948.4:n.919+40T>C
ENST00000262948.9:c.919+40T>C	ENSP00000262948.3:n.919+40T>C
ENST00000394867.8:c.628+40T>C	ENSP00000378336.1:n.628+40T>C
ENST00000595715.1:n.734+40T>C
ENST00000597263.5:n.169+1858T>C
ENST00000599021.1:c.30-1818T>C
ENST00000600584.5:n.1479+40T>C
ENST00000601786.5:n.1220+40T>C
NM_030662.3:c.919+40T>C , LRG_750t1:c.919+40T>C	NP_109587.1:n.919+40T>C
XM_006722799.2:c.705+1858T>C	XP_006722862.1:n.705+1858T>C
XM_011528133.1:c.349+40T>C	XP_011526435.1:n.349+40T>C
XM_017026989.1:c.919+40T>C	XP_016882478.1:n.919+40T>C
XM_017026990.1:c.705+1858T>C	XP_016882479.1:n.705+1858T>C
NM_030662.4:c.919+40T>C MANE Select	NP_109587.1:n.919+40T>C