Canonical Allele Identifier: CA192666406
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs935319299
gnomAD v2: 9-34645573-A-G
gnomAD v3: 9-34645576-A-G
gnomAD v4: 9-34645576-A-G
MyVariant Identifiers: chr9:g.34645573A>G (hg19) chr9:g.34645576A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34645576A>G , CM000671.2:g.34645576A>G GRCh38
NC_000009.11:g.34645573A>G , CM000671.1:g.34645573A>G GRCh37
NC_000009.10:g.34635573A>G NCBI36
NG_009029.1:g.3939A>G
NG_009029.2:g.3988A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000605275.1:n.209-1101A>G
Search 100 bp 5'
Search 100 bp 3'