Canonical Allele Identifier: CA403392680

Gene: MAP2K2

Linked Data

• ClinVar Variation Id: 2981896
• ClinVar RCV Id: RCV003840478
• dbSNP Id: rs768329054
• MyVariant Identifiers: chr19:g.4117535G>A (hg19) ; chr19:g.4117537G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117537G>A , CM000681.2:g.4117537G>A	GRCh38
NC_000019.9:g.4117535G>A , CM000681.1:g.4117535G>A	GRCh37
NC_000019.8:g.4068535G>A	NCBI36
NG_007996.1:g.11592C>T , LRG_750:g.11592C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.624C>T
ENST00000687128.1:n.624C>T
ENST00000262948.10:c.185C>T MANE Select	ENSP00000262948.4:p.Ala62Val
ENST00000262948.9:c.185C>T	ENSP00000262948.3:p.Ala62Val
ENST00000394867.8:c.-107C>T	ENSP00000378336.1:n.-107C>T
ENST00000599345.1:n.382C>T
NM_030662.3:c.185C>T , LRG_750t1:c.185C>T	NP_109587.1:p.Ala62Val
XM_006722799.2:c.185C>T	XP_006722862.1:p.Ala62Val
XM_017026989.1:c.185C>T	XP_016882478.1:p.Ala62Val
XM_017026990.1:c.185C>T	XP_016882479.1:p.Ala62Val
XM_017026991.1:c.185C>T	XP_016882480.1:p.Ala62Val
NM_030662.4:c.185C>T MANE Select	NP_109587.1:p.Ala62Val