Canonical Allele Identifier: CA470467206
Gene: MAT1A HGNC NCBI

Linked Data

gnomAD v4: 10-80273883-C-T
MyVariant Identifiers: chr10:g.82033639C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273883C>T , CM000672.2:g.80273883C>T GRCh38
NC_000010.10:g.82033639C>T , CM000672.1:g.82033639C>T GRCh37
NC_000010.9:g.82023619C>T NCBI36
NG_008083.1:g.20796G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1086G>A MANE Select ENSP00000361287.3:p.Arg362=
ENST00000372213.7:c.1086G>A ENSP00000361287.3:p.Arg362=
ENST00000480845.1:n.318G>A
ENST00000485270.5:n.598G>A
NM_000429.2:c.1086G>A NP_000420.1:p.Arg362=
XM_005269842.3:c.1086G>A XP_005269899.1:p.Arg362=
XM_005269843.3:c.963G>A XP_005269900.1:p.Arg321=
NM_000429.3:c.1086G>A MANE Select NP_000420.1:p.Arg362=
Search 100 bp 5'
Search 100 bp 3'