Canonical Allele Identifier: CA377360572
Gene: MAT1A HGNC NCBI

Linked Data

gnomAD v4: 10-80275031-T-C
MyVariant Identifiers: chr10:g.82034787T>C (hg19) chr10:g.80275031T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275031T>C , CM000672.2:g.80275031T>C GRCh38
NC_000010.10:g.82034787T>C , CM000672.1:g.82034787T>C GRCh37
NC_000010.9:g.82024767T>C NCBI36
NG_008083.1:g.19648A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.937A>G MANE Select ENSP00000361287.3:p.Arg313Gly
ENST00000372213.7:c.937A>G ENSP00000361287.3:p.Arg313Gly
ENST00000480845.1:n.169A>G
ENST00000485270.5:n.449A>G
NM_000429.2:c.937A>G NP_000420.1:p.Arg313Gly
XM_005269842.3:c.937A>G XP_005269899.1:p.Arg313Gly
XM_005269843.3:c.814A>G XP_005269900.1:p.Arg272Gly
NM_000429.3:c.937A>G MANE Select NP_000420.1:p.Arg313Gly
Search 100 bp 5'
Search 100 bp 3'