Canonical Allele Identifier: CA464401739

Gene: GALT

Linked Data

• dbSNP Id: rs1400757380
• gnomAD v3: 9-34646623-G-A
• gnomAD v4: 9-34646623-G-A
• MyVariant Identifiers: chr9:g.34646620G>A (hg19) ; chr9:g.34646623G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646623G>A , CM000671.2:g.34646623G>A	GRCh38
NC_000009.11:g.34646620G>A , CM000671.1:g.34646620G>A	GRCh37
NC_000009.10:g.34636620G>A	NCBI36
NG_009029.1:g.4986G>A
NG_009029.2:g.5035G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000450095.6:c.-284G>A	ENSP00000401956.2:n.-284G>A
ENST00000605275.1:n.209-54G>A
NM_000155.3:c.-82G>A	NP_000146.2:n.-82G>A
NM_001258332.1:c.-284G>A	NP_001245261.1:n.-284G>A