Canonical Allele Identifier: CA505162261

Gene: MAP2K2

Linked Data

• dbSNP Id: rs376988792
• MyVariant Identifiers: chr19:g.4117435G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117437G>C , CM000681.2:g.4117437G>C	GRCh38
NC_000019.9:g.4117435G>C , CM000681.1:g.4117435G>C	GRCh37
NC_000019.8:g.4068435G>C	NCBI36
NG_007996.1:g.11692C>G , LRG_750:g.11692C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.724C>G
ENST00000687128.1:n.724C>G
ENST00000262948.10:c.285C>G MANE Select	ENSP00000262948.4:p.Gly95=
ENST00000262948.9:c.285C>G	ENSP00000262948.3:p.Gly95=
ENST00000394867.8:c.-7C>G	ENSP00000378336.1:n.-7C>G
ENST00000599345.1:n.482C>G
NM_030662.3:c.285C>G , LRG_750t1:c.285C>G	NP_109587.1:p.Gly95=
XM_006722799.2:c.285C>G	XP_006722862.1:p.Gly95=
XM_017026989.1:c.285C>G	XP_016882478.1:p.Gly95=
XM_017026990.1:c.285C>G	XP_016882479.1:p.Gly95=
XM_017026991.1:c.285C>G	XP_016882480.1:p.Gly95=
NM_030662.4:c.285C>G MANE Select	NP_109587.1:p.Gly95=