Canonical Allele Identifier: CA863493172
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1192041385
MyVariant Identifiers: chr9:g.34645594A>T (hg19) chr9:g.34645597A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34645597A>T , CM000671.2:g.34645597A>T GRCh38
NC_000009.11:g.34645594A>T , CM000671.1:g.34645594A>T GRCh37
NC_000009.10:g.34635594A>T NCBI36
NG_009029.1:g.3960A>T
NG_009029.2:g.4009A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000605275.1:n.209-1080A>T
Search 100 bp 5'
Search 100 bp 3'