Canonical Allele Identifier: CA1845634340
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821106892
gnomAD v4: 9-34646616-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646616G>A , CM000671.2:g.34646616G>A GRCh38
NC_000009.11:g.34646613G>A , CM000671.1:g.34646613G>A GRCh37
NC_000009.10:g.34636613G>A NCBI36
NG_009029.1:g.4979G>A
NG_009029.2:g.5028G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-291G>A ENSP00000401956.2:n.-291G>A
ENST00000605275.1:n.209-61G>A
NM_000155.3:c.-89G>A NP_000146.2:n.-89G>A
NM_001258332.1:c.-291G>A NP_001245261.1:n.-291G>A