Canonical Allele Identifier: CA1845632905
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821081867

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34645571A>G , CM000671.2:g.34645571A>G GRCh38
NC_000009.11:g.34645568A>G , CM000671.1:g.34645568A>G GRCh37
NC_000009.10:g.34635568A>G NCBI36
NG_009029.1:g.3934A>G
NG_009029.2:g.3983A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000605275.1:n.209-1106A>G