ClinGen Allele Registry
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Canonical Allele Identifier:
CA10746964
Gene: LINC02770
HGNC
NCBI
Linked Data
dbSNP Id:
rs17403780
gnomAD v2:
1-191939788-T-A
gnomAD v3:
1-191970658-T-A
gnomAD v4:
1-191970658-T-A
MyVariant Identifiers:
chr1:g.191939788T>A (hg19)
chr1:g.191970658T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.191970658T>A , CM000663.2:g.191970658T>A
GRCh38
NC_000001.10:g.191939788T>A , CM000663.1:g.191939788T>A
GRCh37
NC_000001.9:g.190206411T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_001737812.2:n.92+5245T>A
Search 100 bp 5'
Search 100 bp 3'