Canonical Allele Identifier: CA2722248469
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs2132701803
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275243T>G , CM000672.2:g.80275243T>G GRCh38
NC_000010.10:g.82034999T>G , CM000672.1:g.82034999T>G GRCh37
NC_000010.9:g.82024979T>G NCBI36
NG_008083.1:g.19436A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.769-44A>C MANE Select ENSP00000361287.3:n.769-44A>C
ENST00000372213.7:c.769-44A>C ENSP00000361287.3:n.769-44A>C
ENST00000485270.5:n.237A>C
NM_000429.2:c.769-44A>C NP_000420.1:n.769-44A>C
XM_005269842.3:c.769-44A>C XP_005269899.1:n.769-44A>C
XM_005269843.3:c.646-44A>C XP_005269900.1:n.646-44A>C
NM_000429.3:c.769-44A>C MANE Select NP_000420.1:n.769-44A>C
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