Canonical Allele Identifier: CA2689808302
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34646610-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646610C>T , CM000671.2:g.34646610C>T GRCh38
NC_000009.11:g.34646607C>T , CM000671.1:g.34646607C>T GRCh37
NC_000009.10:g.34636607C>T NCBI36
NG_009029.1:g.4973C>T
NG_009029.2:g.5022C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-297C>T ENSP00000401956.2:n.-297C>T
ENST00000605275.1:n.209-67C>T
NM_000155.3:c.-95C>T NP_000146.2:n.-95C>T
NM_001258332.1:c.-297C>T NP_001245261.1:n.-297C>T
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