Canonical Allele Identifier: CA631537748

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1384481669
• gnomAD v2: 19-4094265-T-C
• gnomAD v3: 19-4094267-T-C
• gnomAD v4: 19-4094267-T-C
• MyVariant Identifiers: chr19:g.4094265T>C (hg19) ; chr19:g.4094267T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094267T>C , CM000681.2:g.4094267T>C	GRCh38
NC_000019.9:g.4094265T>C , CM000681.1:g.4094265T>C	GRCh37
NC_000019.8:g.4045265T>C	NCBI36
NG_007996.1:g.34862A>G , LRG_750:g.34862A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1531+186A>G
ENST00000688002.1:n.3243+186A>G
ENST00000688751.1:n.228+186A>G
ENST00000689792.1:n.996+186A>G
ENST00000262948.10:c.1092+186A>G MANE Select	ENSP00000262948.4:n.1092+186A>G
ENST00000262948.9:c.1092+186A>G	ENSP00000262948.3:n.1092+186A>G
ENST00000394867.8:c.801+186A>G	ENSP00000378336.1:n.801+186A>G
ENST00000597263.5:n.277+186A>G
ENST00000599021.1:c.202+186A>G
ENST00000600584.5:n.2541+186A>G
ENST00000601786.5:n.1393+186A>G
NM_030662.3:c.1092+186A>G , LRG_750t1:c.1092+186A>G	NP_109587.1:n.1092+186A>G
XM_006722799.2:c.813+186A>G	XP_006722862.1:n.813+186A>G
XM_011528133.1:c.522+186A>G	XP_011526435.1:n.522+186A>G
NM_030662.4:c.1092+186A>G MANE Select	NP_109587.1:n.1092+186A>G