Canonical Allele Identifier: CA1976060338
Gene: GLYAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.58705326C>T , CM000673.2:g.58705326C>T GRCh38
NC_000011.9:g.58472799C>T , CM000673.1:g.58472799C>T GRCh37
NC_000011.8:g.58229375C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000586098.1:c.90+7434G>A