Canonical Allele Identifier: CA377360829
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82034909C>G (hg19) chr10:g.80275153C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275153C>G , CM000672.2:g.80275153C>G GRCh38
NC_000010.10:g.82034909C>G , CM000672.1:g.82034909C>G GRCh37
NC_000010.9:g.82024889C>G NCBI36
NG_008083.1:g.19526G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.815G>C MANE Select ENSP00000361287.3:p.Gly272Ala
ENST00000372213.7:c.815G>C ENSP00000361287.3:p.Gly272Ala
ENST00000480845.1:n.47G>C
ENST00000485270.5:n.327G>C
NM_000429.2:c.815G>C NP_000420.1:p.Gly272Ala
XM_005269842.3:c.815G>C XP_005269899.1:p.Gly272Ala
XM_005269843.3:c.692G>C XP_005269900.1:p.Gly231Ala
NM_000429.3:c.815G>C MANE Select NP_000420.1:p.Gly272Ala
Search 100 bp 5'
Search 100 bp 3'