Canonical Allele Identifier: CA223178830

Gene: GLYAT

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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