Canonical Allele Identifier: CA2576573164

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145049252
• gnomAD v4: 19-4099155-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099155C>T , CM000681.2:g.4099155C>T	GRCh38
NC_000019.9:g.4099153C>T , CM000681.1:g.4099153C>T	GRCh37
NC_000019.8:g.4050153C>T	NCBI36
NG_007996.1:g.29974G>A , LRG_750:g.29974G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+46G>A
ENST00000687128.1:n.1404G>A
ENST00000688002.1:n.1259G>A
ENST00000689792.1:n.823+46G>A
ENST00000262948.10:c.919+46G>A MANE Select	ENSP00000262948.4:n.919+46G>A
ENST00000262948.9:c.919+46G>A	ENSP00000262948.3:n.919+46G>A
ENST00000394867.8:c.628+46G>A	ENSP00000378336.1:n.628+46G>A
ENST00000595715.1:n.734+46G>A
ENST00000597263.5:n.169+1864G>A
ENST00000599021.1:c.30-1812G>A
ENST00000600584.5:n.1479+46G>A
ENST00000601786.5:n.1220+46G>A
NM_030662.3:c.919+46G>A , LRG_750t1:c.919+46G>A	NP_109587.1:n.919+46G>A
XM_006722799.2:c.705+1864G>A	XP_006722862.1:n.705+1864G>A
XM_011528133.1:c.349+46G>A	XP_011526435.1:n.349+46G>A
XM_017026989.1:c.919+46G>A	XP_016882478.1:n.919+46G>A
XM_017026990.1:c.705+1864G>A	XP_016882479.1:n.705+1864G>A
NM_030662.4:c.919+46G>A MANE Select	NP_109587.1:n.919+46G>A