Canonical Allele Identifier: CA2703126887
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs2106893207

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124090A>C , CM000665.2:g.87124090A>C GRCh38
NC_000003.11:g.87173240A>C , CM000665.1:g.87173240A>C GRCh37
NC_000003.10:g.87255930A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104153.1:n.329-30248A>C