Canonical Allele Identifier: CA2689808292
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34646607-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646607A>C , CM000671.2:g.34646607A>C GRCh38
NC_000009.11:g.34646604A>C , CM000671.1:g.34646604A>C GRCh37
NC_000009.10:g.34636604A>C NCBI36
NG_009029.1:g.4970A>C
NG_009029.2:g.5019A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-300A>C ENSP00000401956.2:n.-300A>C
ENST00000605275.1:n.209-70A>C
NM_000155.3:c.-98A>C NP_000146.2:n.-98A>C
NM_001258332.1:c.-300A>C NP_001245261.1:n.-300A>C
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