Canonical Allele Identifier: CA403386518

Gene: MAP2K2

Linked Data

• ClinVar Variation Id: 3228057
• ClinVar RCV Id: RCV004517801
• dbSNP Id: rs1377552828
• gnomAD v2: 19-4099324-T-C
• gnomAD v4: 19-4099326-T-C
• MyVariant Identifiers: chr19:g.4099324T>C (hg19) ; chr19:g.4099326T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099326T>C , CM000681.2:g.4099326T>C	GRCh38
NC_000019.9:g.4099324T>C , CM000681.1:g.4099324T>C	GRCh37
NC_000019.8:g.4050324T>C	NCBI36
NG_007996.1:g.29803A>G , LRG_750:g.29803A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1233A>G
ENST00000687128.1:n.1233A>G
ENST00000688002.1:n.1088A>G
ENST00000689792.1:n.698A>G
ENST00000262948.10:c.794A>G MANE Select	ENSP00000262948.4:p.Tyr265Cys
ENST00000262948.9:c.794A>G	ENSP00000262948.3:p.Tyr265Cys
ENST00000394867.8:c.503A>G	ENSP00000378336.1:p.Tyr168Cys
ENST00000593364.5:n.741A>G
ENST00000595715.1:n.609A>G
ENST00000597263.5:n.169+1693A>G
ENST00000599021.1:c.29+1693A>G
ENST00000600584.5:n.1354A>G
ENST00000601786.5:n.1095A>G
NM_030662.3:c.794A>G , LRG_750t1:c.794A>G	NP_109587.1:p.Tyr265Cys
XM_006722799.2:c.705+1693A>G	XP_006722862.1:n.705+1693A>G
XM_011528133.1:c.224A>G	XP_011526435.1:p.Tyr75Cys
XM_017026989.1:c.794A>G	XP_016882478.1:p.Tyr265Cys
XM_017026990.1:c.705+1693A>G	XP_016882479.1:n.705+1693A>G
NM_030662.4:c.794A>G MANE Select	NP_109587.1:p.Tyr265Cys