Canonical Allele Identifier: CA2689808326
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34646622-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646622C>A , CM000671.2:g.34646622C>A GRCh38
NC_000009.11:g.34646619C>A , CM000671.1:g.34646619C>A GRCh37
NC_000009.10:g.34636619C>A NCBI36
NG_009029.1:g.4985C>A
NG_009029.2:g.5034C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-285C>A ENSP00000401956.2:n.-285C>A
ENST00000605275.1:n.209-55C>A
NM_000155.3:c.-83C>A NP_000146.2:n.-83C>A
NM_001258332.1:c.-285C>A NP_001245261.1:n.-285C>A
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