Canonical Allele Identifier: CA79020305
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs764908969
gnomAD v3: 3-87124095-A-G
gnomAD v4: 3-87124095-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124095A>G , CM000665.2:g.87124095A>G GRCh38
NC_000003.11:g.87173245A>G , CM000665.1:g.87173245A>G GRCh37
NC_000003.10:g.87255935A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104153.1:n.329-30243A>G