Canonical Allele Identifier: CA2579370997
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34646613-C-A

Genomic Alleles

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

Transcript Alleles

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