Canonical Allele Identifier: CA2013297303
Gene: GALNT8 HGNC NCBI

Linked Data

dbSNP Id: rs191572027
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4754168G>A , CM000674.2:g.4754168G>A GRCh38
NC_000012.11:g.4863334G>A , CM000674.1:g.4863334G>A GRCh37
NC_000012.10:g.4733595G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000252318.7:c.1174-6790G>A MANE Select ENSP00000252318.2:n.1174-6790G>A
ENST00000648836.1:c.964-6790G>A ENSP00000497305.1:n.964-6790G>A
ENST00000648865.1:n.26-6790G>A
ENST00000252318.6:c.1174-6790G>A ENSP00000252318.2:n.1174-6790G>A
NM_017417.1:c.1174-6790G>A NP_059113.1:n.1174-6790G>A
NM_017417.2:c.1174-6790G>A MANE Select NP_059113.1:n.1174-6790G>A
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