Canonical Allele Identifier: CA1845634327
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821106719
gnomAD v4: 9-34646613-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646613C>T , CM000671.2:g.34646613C>T GRCh38
NC_000009.11:g.34646610C>T , CM000671.1:g.34646610C>T GRCh37
NC_000009.10:g.34636610C>T NCBI36
NG_009029.1:g.4976C>T
NG_009029.2:g.5025C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450095.6:c.-294C>T ENSP00000401956.2:n.-294C>T
ENST00000605275.1:n.209-64C>T
NM_000155.3:c.-92C>T NP_000146.2:n.-92C>T
NM_001258332.1:c.-294C>T NP_001245261.1:n.-294C>T