ClinGen Allele Registry
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Canonical Allele Identifier:
CA13325541
Gene: LINC02627
HGNC
NCBI
Linked Data
dbSNP Id:
rs17119461
gnomAD v2:
10-107516352-T-C
gnomAD v3:
10-105756594-T-C
gnomAD v4:
10-105756594-T-C
MyVariant Identifiers:
chr10:g.107516352T>C (hg19)
chr10:g.105756594T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.105756594T>C , CM000672.2:g.105756594T>C
GRCh38
NC_000010.10:g.107516352T>C , CM000672.1:g.107516352T>C
GRCh37
NC_000010.9:g.107506342T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_120625.1:n.430+61324A>G
Search 100 bp 5'
Search 100 bp 3'