Canonical Allele Identifier: CA2579371001
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34646619-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646619C>T , CM000671.2:g.34646619C>T GRCh38
NC_000009.11:g.34646616C>T , CM000671.1:g.34646616C>T GRCh37
NC_000009.10:g.34636616C>T NCBI36
NG_009029.1:g.4982C>T
NG_009029.2:g.5031C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-288C>T ENSP00000401956.2:n.-288C>T
ENST00000605275.1:n.209-58C>T
NM_000155.3:c.-86C>T NP_000146.2:n.-86C>T
NM_001258332.1:c.-288C>T NP_001245261.1:n.-288C>T
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