Canonical Allele Identifier: CA192668862

Gene: GALT

Linked Data

• dbSNP Id: rs888379555
• gnomAD v4: 9-34646536-A-C
• MyVariant Identifiers: chr9:g.34646533A>C (hg19) ; chr9:g.34646536A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646536A>C , CM000671.2:g.34646536A>C	GRCh38
NC_000009.11:g.34646533A>C , CM000671.1:g.34646533A>C	GRCh37
NC_000009.10:g.34636533A>C	NCBI36
NG_009029.1:g.4899A>C
NG_009029.2:g.4948A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000605275.1:n.209-141A>C