Canonical Allele Identifier: CA470467396
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82034920C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275164C>G , CM000672.2:g.80275164C>G GRCh38
NC_000010.10:g.82034920C>G , CM000672.1:g.82034920C>G GRCh37
NC_000010.9:g.82024900C>G NCBI36
NG_008083.1:g.19515G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.804G>C MANE Select ENSP00000361287.3:p.Val268=
ENST00000372213.7:c.804G>C ENSP00000361287.3:p.Val268=
ENST00000480845.1:n.36G>C
ENST00000485270.5:n.316G>C
NM_000429.2:c.804G>C NP_000420.1:p.Val268=
XM_005269842.3:c.804G>C XP_005269899.1:p.Val268=
XM_005269843.3:c.681G>C XP_005269900.1:p.Val227=
NM_000429.3:c.804G>C MANE Select NP_000420.1:p.Val268=