Canonical Allele Identifier: CA544782017
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1477657239
gnomAD v2: 3-87173187-T-C
gnomAD v3: 3-87124037-T-C
gnomAD v4: 3-87124037-T-C
MyVariant Identifiers: chr3:g.87173187T>C (hg19) chr3:g.87124037T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124037T>C , CM000665.2:g.87124037T>C GRCh38
NC_000003.11:g.87173187T>C , CM000665.1:g.87173187T>C GRCh37
NC_000003.10:g.87255877T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30301T>C
Search 100 bp 5'
Search 100 bp 3'