Canonical Allele Identifier: CA2601324835
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs2106893283
gnomAD v3: 3-87124177-C-T
gnomAD v4: 3-87124177-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124177C>T , CM000665.2:g.87124177C>T GRCh38
NC_000003.11:g.87173327C>T , CM000665.1:g.87173327C>T GRCh37
NC_000003.10:g.87256017C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30161C>T