Canonical Allele Identifier: CA911624796
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1227571479
gnomAD v3: 3-87124175-T-C
gnomAD v4: 3-87124175-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124175T>C , CM000665.2:g.87124175T>C GRCh38
NC_000003.11:g.87173325T>C , CM000665.1:g.87173325T>C GRCh37
NC_000003.10:g.87256015T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30163T>C