Canonical Allele Identifier: CA210322879
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs1014445385
gnomAD v3: 10-80275406-C-T
gnomAD v4: 10-80275406-C-T
MyVariant Identifiers: chr10:g.82035162C>T (hg19) chr10:g.80275406C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275406C>T , CM000672.2:g.80275406C>T GRCh38
NC_000010.10:g.82035162C>T , CM000672.1:g.82035162C>T GRCh37
NC_000010.9:g.82025142C>T NCBI36
NG_008083.1:g.19273G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.769-207G>A MANE Select ENSP00000361287.3:n.769-207G>A
ENST00000372213.7:c.769-207G>A ENSP00000361287.3:n.769-207G>A
ENST00000485270.5:n.74G>A
NM_000429.2:c.769-207G>A NP_000420.1:n.769-207G>A
XM_005269842.3:c.769-207G>A XP_005269899.1:n.769-207G>A
XM_005269843.3:c.646-207G>A XP_005269900.1:n.646-207G>A
NM_000429.3:c.769-207G>A MANE Select NP_000420.1:n.769-207G>A
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