ClinGen Allele Registry
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Canonical Allele Identifier:
CA850291727
Gene: LINC03021
HGNC
NCBI
Linked Data
dbSNP Id:
rs1446828173
gnomAD v3:
8-2649417-T-C
gnomAD v4:
8-2649417-T-C
MyVariant Identifiers:
chr8:g.2506934T>C (hg19)
chr8:g.2649417T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.2649417T>C , CM000670.2:g.2649417T>C
GRCh38
NC_000008.10:g.2506934T>C , CM000670.1:g.2506934T>C
GRCh37
NC_000008.9:g.2494341T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_125425.1:n.238+25313A>G
Search 100 bp 5'
Search 100 bp 3'