Canonical Allele Identifier: CA2689808290
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34646605-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646605C>A , CM000671.2:g.34646605C>A GRCh38
NC_000009.11:g.34646602C>A , CM000671.1:g.34646602C>A GRCh37
NC_000009.10:g.34636602C>A NCBI36
NG_009029.1:g.4968C>A
NG_009029.2:g.5017C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-302C>A ENSP00000401956.2:n.-302C>A
ENST00000605275.1:n.209-72C>A
NM_000155.3:c.-100C>A NP_000146.2:n.-100C>A
NM_001258332.1:c.-302C>A NP_001245261.1:n.-302C>A