Canonical Allele Identifier: CA79020306
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs770772093
gnomAD v2: 3-87173248-T-C
gnomAD v3: 3-87124098-T-C
gnomAD v4: 3-87124098-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124098T>C , CM000665.2:g.87124098T>C GRCh38
NC_000003.11:g.87173248T>C , CM000665.1:g.87173248T>C GRCh37
NC_000003.10:g.87255938T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104153.1:n.329-30240T>C