Canonical Allele Identifier: CA2689808337
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34646625-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646625G>T , CM000671.2:g.34646625G>T GRCh38
NC_000009.11:g.34646622G>T , CM000671.1:g.34646622G>T GRCh37
NC_000009.10:g.34636622G>T NCBI36
NG_009029.1:g.4988G>T
NG_009029.2:g.5037G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-282G>T ENSP00000401956.2:n.-282G>T
ENST00000605275.1:n.209-52G>T
NM_000155.3:c.-80G>T NP_000146.2:n.-80G>T
NM_001258332.1:c.-282G>T NP_001245261.1:n.-282G>T