Canonical Allele Identifier: CA631537841

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1345837619
• gnomAD v2: 19-4094508-A-G
• gnomAD v4: 19-4094510-A-G
• MyVariant Identifiers: chr19:g.4094508A>G (hg19) ; chr19:g.4094510A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094510A>G , CM000681.2:g.4094510A>G	GRCh38
NC_000019.9:g.4094508A>G , CM000681.1:g.4094508A>G	GRCh37
NC_000019.8:g.4045508A>G	NCBI36
NG_007996.1:g.34619T>C , LRG_750:g.34619T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-12T>C
ENST00000688002.1:n.3198-12T>C
ENST00000688751.1:n.183-12T>C
ENST00000689792.1:n.951-12T>C
ENST00000262948.10:c.1047-12T>C MANE Select	ENSP00000262948.4:n.1047-12T>C
ENST00000262948.9:c.1047-12T>C	ENSP00000262948.3:n.1047-12T>C
ENST00000394867.8:c.756-12T>C	ENSP00000378336.1:n.756-12T>C
ENST00000597263.5:n.232-12T>C
ENST00000599021.1:c.157-12T>C
ENST00000600584.5:n.2484T>C
ENST00000601786.5:n.1348-12T>C
NM_030662.3:c.1047-12T>C , LRG_750t1:c.1047-12T>C	NP_109587.1:n.1047-12T>C
XM_006722799.2:c.768-12T>C	XP_006722862.1:n.768-12T>C
XM_011528133.1:c.477-12T>C	XP_011526435.1:n.477-12T>C
NM_030662.4:c.1047-12T>C MANE Select	NP_109587.1:n.1047-12T>C