Canonical Allele Identifier: CA1845634338
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821106838

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646615G>C , CM000671.2:g.34646615G>C GRCh38
NC_000009.11:g.34646612G>C , CM000671.1:g.34646612G>C GRCh37
NC_000009.10:g.34636612G>C NCBI36
NG_009029.1:g.4978G>C
NG_009029.2:g.5027G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-292G>C ENSP00000401956.2:n.-292G>C
ENST00000605275.1:n.209-62G>C
NM_000155.3:c.-90G>C NP_000146.2:n.-90G>C
NM_001258332.1:c.-292G>C NP_001245261.1:n.-292G>C