Canonical Allele Identifier: CA863493831

Gene: GALT

Linked Data

• dbSNP Id: rs1299883909
• gnomAD v3: 9-34646620-G-A
• gnomAD v4: 9-34646620-G-A
• MyVariant Identifiers: chr9:g.34646617G>A (hg19) ; chr9:g.34646620G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646620G>A , CM000671.2:g.34646620G>A	GRCh38
NC_000009.11:g.34646617G>A , CM000671.1:g.34646617G>A	GRCh37
NC_000009.10:g.34636617G>A	NCBI36
NG_009029.1:g.4983G>A
NG_009029.2:g.5032G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000450095.6:c.-287G>A	ENSP00000401956.2:n.-287G>A
ENST00000605275.1:n.209-57G>A
NM_000155.3:c.-85G>A	NP_000146.2:n.-85G>A
NM_001258332.1:c.-287G>A	NP_001245261.1:n.-287G>A