Canonical Allele Identifier: CA863493661

Gene: GALT

Linked Data

• dbSNP Id: rs1236586713
• MyVariant Identifiers: chr9:g.34646389C>A (hg19) ; chr9:g.34646392C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646392C>A , CM000671.2:g.34646392C>A	GRCh38
NC_000009.11:g.34646389C>A , CM000671.1:g.34646389C>A	GRCh37
NC_000009.10:g.34636389C>A	NCBI36
NG_009029.1:g.4755C>A
NG_009029.2:g.4804C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000605275.1:n.209-285C>A