Canonical Allele Identifier: CA863493840
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1358634638
gnomAD v4: 9-34646625-G-A
MyVariant Identifiers: chr9:g.34646622G>A (hg19) chr9:g.34646625G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646625G>A , CM000671.2:g.34646625G>A GRCh38
NC_000009.11:g.34646622G>A , CM000671.1:g.34646622G>A GRCh37
NC_000009.10:g.34636622G>A NCBI36
NG_009029.1:g.4988G>A
NG_009029.2:g.5037G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-282G>A ENSP00000401956.2:n.-282G>A
ENST00000605275.1:n.209-52G>A
NM_000155.3:c.-80G>A NP_000146.2:n.-80G>A
NM_001258332.1:c.-282G>A NP_001245261.1:n.-282G>A
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