Canonical Allele Identifier: CA2689808293
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34646608-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646608A>G , CM000671.2:g.34646608A>G GRCh38
NC_000009.11:g.34646605A>G , CM000671.1:g.34646605A>G GRCh37
NC_000009.10:g.34636605A>G NCBI36
NG_009029.1:g.4971A>G
NG_009029.2:g.5020A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-299A>G ENSP00000401956.2:n.-299A>G
ENST00000605275.1:n.209-69A>G
NM_000155.3:c.-97A>G NP_000146.2:n.-97A>G
NM_001258332.1:c.-299A>G NP_001245261.1:n.-299A>G