Canonical Allele Identifier: CA668888705
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs1321193746
gnomAD v3: 10-80280448-T-G
gnomAD v4: 10-80280448-T-G
MyVariant Identifiers: chr10:g.82040204T>G (hg19) chr10:g.80280448T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280448T>G , CM000672.2:g.80280448T>G GRCh38
NC_000010.10:g.82040204T>G , CM000672.1:g.82040204T>G GRCh37
NC_000010.9:g.82030184T>G NCBI36
NG_008083.1:g.14231A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406-132A>C MANE Select ENSP00000361287.3:n.406-132A>C
ENST00000372213.7:c.406-132A>C ENSP00000361287.3:n.406-132A>C
ENST00000455001.1:c.217-132A>C ENSP00000414961.1:n.217-132A>C
NM_000429.2:c.406-132A>C NP_000420.1:n.406-132A>C
XM_005269842.3:c.406-132A>C XP_005269899.1:n.406-132A>C
XM_005269843.3:c.283-132A>C XP_005269900.1:n.283-132A>C
NM_000429.3:c.406-132A>C MANE Select NP_000420.1:n.406-132A>C
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