Canonical Allele Identifier: CA304447219

Gene: MAP2K2

Linked Data

• dbSNP Id: rs938236465
• gnomAD v3: 19-4094718-C-T
• gnomAD v4: 19-4094718-C-T
• MyVariant Identifiers: chr19:g.4094716C>T (hg19) ; chr19:g.4094718C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094718C>T , CM000681.2:g.4094718C>T	GRCh38
NC_000019.9:g.4094716C>T , CM000681.1:g.4094716C>T	GRCh37
NC_000019.8:g.4045716C>T	NCBI36
NG_007996.1:g.34411G>A , LRG_750:g.34411G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-220G>A
ENST00000688002.1:n.3198-220G>A
ENST00000688751.1:n.183-220G>A
ENST00000689792.1:n.951-220G>A
ENST00000262948.10:c.1047-220G>A MANE Select	ENSP00000262948.4:n.1047-220G>A
ENST00000262948.9:c.1047-220G>A	ENSP00000262948.3:n.1047-220G>A
ENST00000394867.8:c.756-220G>A	ENSP00000378336.1:n.756-220G>A
ENST00000597263.5:n.232-220G>A
ENST00000599021.1:c.157-220G>A
ENST00000600584.5:n.2276G>A
ENST00000601786.5:n.1348-220G>A
NM_030662.3:c.1047-220G>A , LRG_750t1:c.1047-220G>A	NP_109587.1:n.1047-220G>A
XM_006722799.2:c.768-220G>A	XP_006722862.1:n.768-220G>A
XM_011528133.1:c.477-220G>A	XP_011526435.1:n.477-220G>A
XM_017026989.1:c.1375G>A	XP_016882478.1:p.Ala459Thr
XM_017026990.1:c.1096G>A	XP_016882479.1:p.Ala366Thr
NM_030662.4:c.1047-220G>A MANE Select	NP_109587.1:n.1047-220G>A