Canonical Allele Identifier: CA2689808319
Gene: GALT HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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