Canonical Allele Identifier: CA470467386
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82034899C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275143C>T , CM000672.2:g.80275143C>T GRCh38
NC_000010.10:g.82034899C>T , CM000672.1:g.82034899C>T GRCh37
NC_000010.9:g.82024879C>T NCBI36
NG_008083.1:g.19536G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.825G>A MANE Select ENSP00000361287.3:p.Gly275=
ENST00000372213.7:c.825G>A ENSP00000361287.3:p.Gly275=
ENST00000480845.1:n.57G>A
ENST00000485270.5:n.337G>A
NM_000429.2:c.825G>A NP_000420.1:p.Gly275=
XM_005269842.3:c.825G>A XP_005269899.1:p.Gly275=
XM_005269843.3:c.702G>A XP_005269900.1:p.Gly234=
NM_000429.3:c.825G>A MANE Select NP_000420.1:p.Gly275=