Canonical Allele Identifier: CA470467404

Gene: MAT1A

Linked Data

• dbSNP Id: rs1248281031
• MyVariant Identifiers: chr10:g.82034932A>G (hg19) ; chr10:g.80275176A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80275176A>G , CM000672.2:g.80275176A>G	GRCh38
NC_000010.10:g.82034932A>G , CM000672.1:g.82034932A>G	GRCh37
NC_000010.9:g.82024912A>G	NCBI36
NG_008083.1:g.19503T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.792T>C MANE Select	ENSP00000361287.3:p.Arg264=
ENST00000372213.7:c.792T>C	ENSP00000361287.3:p.Arg264=
ENST00000480845.1:n.24T>C
ENST00000485270.5:n.304T>C
NM_000429.2:c.792T>C	NP_000420.1:p.Arg264=
XM_005269842.3:c.792T>C	XP_005269899.1:p.Arg264=
XM_005269843.3:c.669T>C	XP_005269900.1:p.Arg223=
NM_000429.3:c.792T>C MANE Select	NP_000420.1:p.Arg264=