Canonical Allele Identifier: CA470468246
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82039976T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280220T>G , CM000672.2:g.80280220T>G GRCh38
NC_000010.10:g.82039976T>G , CM000672.1:g.82039976T>G GRCh37
NC_000010.9:g.82029956T>G NCBI36
NG_008083.1:g.14459A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.502A>C MANE Select ENSP00000361287.3:p.Arg168=
ENST00000372213.7:c.502A>C ENSP00000361287.3:p.Arg168=
ENST00000455001.1:c.313A>C ENSP00000414961.1:p.Arg105=
NM_000429.2:c.502A>C NP_000420.1:p.Arg168=
XM_005269842.3:c.502A>C XP_005269899.1:p.Arg168=
XM_005269843.3:c.379A>C XP_005269900.1:p.Arg127=
NM_000429.3:c.502A>C MANE Select NP_000420.1:p.Arg168=