Canonical Allele Identifier: CA631537740

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1190695519
• gnomAD v2: 19-4094192-C-G
• gnomAD v3: 19-4094194-C-G
• gnomAD v4: 19-4094194-C-G
• MyVariant Identifiers: chr19:g.4094192C>G (hg19) ; chr19:g.4094194C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094194C>G , CM000681.2:g.4094194C>G	GRCh38
NC_000019.9:g.4094192C>G , CM000681.1:g.4094192C>G	GRCh37
NC_000019.8:g.4045192C>G	NCBI36
NG_007996.1:g.34935G>C , LRG_750:g.34935G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1531+259G>C
ENST00000688002.1:n.3243+259G>C
ENST00000688751.1:n.228+259G>C
ENST00000689792.1:n.996+259G>C
ENST00000262948.10:c.1092+259G>C MANE Select	ENSP00000262948.4:n.1092+259G>C
ENST00000262948.9:c.1092+259G>C	ENSP00000262948.3:n.1092+259G>C
ENST00000394867.8:c.801+259G>C	ENSP00000378336.1:n.801+259G>C
ENST00000597263.5:n.277+259G>C
ENST00000599021.1:c.202+259G>C
ENST00000600584.5:n.2541+259G>C
ENST00000601786.5:n.1393+259G>C
NM_030662.3:c.1092+259G>C , LRG_750t1:c.1092+259G>C	NP_109587.1:n.1092+259G>C
XM_006722799.2:c.813+259G>C	XP_006722862.1:n.813+259G>C
XM_011528133.1:c.522+259G>C	XP_011526435.1:n.522+259G>C
NM_030662.4:c.1092+259G>C MANE Select	NP_109587.1:n.1092+259G>C