Canonical Allele Identifier: CA2719565859
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs2132339011

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34645603A>G , CM000671.2:g.34645603A>G GRCh38
NC_000009.11:g.34645600A>G , CM000671.1:g.34645600A>G GRCh37
NC_000009.10:g.34635600A>G NCBI36
NG_009029.1:g.3966A>G
NG_009029.2:g.4015A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000605275.1:n.209-1074A>G