ClinGen Allele Registry
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Canonical Allele Identifier:
CA170532308
Gene: LINC03021
HGNC
NCBI
Linked Data
dbSNP Id:
rs950594477
gnomAD v2:
8-2507012-C-T
gnomAD v3:
8-2649495-C-T
gnomAD v4:
8-2649495-C-T
MyVariant Identifiers:
chr8:g.2507012C>T (hg19)
chr8:g.2649495C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.2649495C>T , CM000670.2:g.2649495C>T
GRCh38
NC_000008.10:g.2507012C>T , CM000670.1:g.2507012C>T
GRCh37
NC_000008.9:g.2494419C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_125425.1:n.238+25235G>A
Search 100 bp 5'
Search 100 bp 3'