Canonical Allele Identifier: CA985878204

Gene: LINC01483

Linked Data

• dbSNP Id: rs974078298
• gnomAD v3: 17-69854937-C-A
• gnomAD v4: 17-69854937-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69854937C>A , CM000679.2:g.69854937C>A	GRCh38
NC_000017.10:g.67851078C>A , CM000679.1:g.67851078C>A	GRCh37
NC_000017.9:g.65362673C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109971.1:n.363+9451C>A
NR_109972.1:n.363+9451C>A