ClinGen Allele Registry
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Canonical Allele Identifier:
CA850291761
Gene: LINC03021
HGNC
NCBI
Linked Data
dbSNP Id:
rs1471901122
gnomAD v3:
8-2649487-A-G
gnomAD v4:
8-2649487-A-G
MyVariant Identifiers:
chr8:g.2507004A>G (hg19)
chr8:g.2649487A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.2649487A>G , CM000670.2:g.2649487A>G
GRCh38
NC_000008.10:g.2507004A>G , CM000670.1:g.2507004A>G
GRCh37
NC_000008.9:g.2494411A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_125425.1:n.238+25243T>C
Search 100 bp 5'
Search 100 bp 3'