Canonical Allele Identifier: CA377360770
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82034886C>T (hg19) chr10:g.80275130C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275130C>T , CM000672.2:g.80275130C>T GRCh38
NC_000010.10:g.82034886C>T , CM000672.1:g.82034886C>T GRCh37
NC_000010.9:g.82024866C>T NCBI36
NG_008083.1:g.19549G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.838G>A MANE Select ENSP00000361287.3:p.Gly280Arg
ENST00000372213.7:c.838G>A ENSP00000361287.3:p.Gly280Arg
ENST00000480845.1:n.70G>A
ENST00000485270.5:n.350G>A
NM_000429.2:c.838G>A NP_000420.1:p.Gly280Arg
XM_005269842.3:c.838G>A XP_005269899.1:p.Gly280Arg
XM_005269843.3:c.715G>A XP_005269900.1:p.Gly239Arg
NM_000429.3:c.838G>A MANE Select NP_000420.1:p.Gly280Arg
Search 100 bp 5'
Search 100 bp 3'