Canonical Allele Identifier: CA2689808291
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34646606-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646606C>A , CM000671.2:g.34646606C>A GRCh38
NC_000009.11:g.34646603C>A , CM000671.1:g.34646603C>A GRCh37
NC_000009.10:g.34636603C>A NCBI36
NG_009029.1:g.4969C>A
NG_009029.2:g.5018C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-301C>A ENSP00000401956.2:n.-301C>A
ENST00000605275.1:n.209-71C>A
NM_000155.3:c.-99C>A NP_000146.2:n.-99C>A
NM_001258332.1:c.-301C>A NP_001245261.1:n.-301C>A
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