Canonical Allele Identifier: CA377361565
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82036142C>G (hg19) chr10:g.80276386C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80276386C>G , CM000672.2:g.80276386C>G GRCh38
NC_000010.10:g.82036142C>G , CM000672.1:g.82036142C>G GRCh37
NC_000010.9:g.82026122C>G NCBI36
NG_008083.1:g.18293G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.758G>C MANE Select ENSP00000361287.3:p.Gly253Ala
ENST00000372213.7:c.758G>C ENSP00000361287.3:p.Gly253Ala
NM_000429.2:c.758G>C NP_000420.1:p.Gly253Ala
XM_005269842.3:c.758G>C XP_005269899.1:p.Gly253Ala
XM_005269843.3:c.635G>C XP_005269900.1:p.Gly212Ala
NM_000429.3:c.758G>C MANE Select NP_000420.1:p.Gly253Ala
Search 100 bp 5'
Search 100 bp 3'