Canonical Allele Identifier: CA882251349

Gene: MAP2K2

Linked Data

• dbSNP Id: rs769291518
• gnomAD v3: 19-4110458-T-G
• gnomAD v4: 19-4110458-T-G
• MyVariant Identifiers: chr19:g.4110456T>G (hg19) ; chr19:g.4110458T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4110458T>G , CM000681.2:g.4110458T>G	GRCh38
NC_000019.9:g.4110456T>G , CM000681.1:g.4110456T>G	GRCh37
NC_000019.8:g.4061456T>G	NCBI36
NG_007996.1:g.18671A>C , LRG_750:g.18671A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.889+51A>C
ENST00000687128.1:n.889+51A>C
ENST00000262948.10:c.450+51A>C MANE Select	ENSP00000262948.4:n.450+51A>C
ENST00000262948.9:c.450+51A>C	ENSP00000262948.3:n.450+51A>C
ENST00000394867.8:c.159+51A>C	ENSP00000378336.1:n.159+51A>C
ENST00000599345.1:n.647+51A>C
NM_030662.3:c.450+51A>C , LRG_750t1:c.450+51A>C	NP_109587.1:n.450+51A>C
XM_006722799.2:c.450+51A>C	XP_006722862.1:n.450+51A>C
XM_017026989.1:c.450+51A>C	XP_016882478.1:n.450+51A>C
XM_017026990.1:c.450+51A>C	XP_016882479.1:n.450+51A>C
XM_017026991.1:c.450+51A>C	XP_016882480.1:n.450+51A>C
NM_030662.4:c.450+51A>C MANE Select	NP_109587.1:n.450+51A>C