ClinGen Allele Registry
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Canonical Allele Identifier:
CA13648521
Gene: LINC01465
HGNC
NCBI
Linked Data
dbSNP Id:
rs10877887
gnomAD v2:
12-62997180-T-C
gnomAD v3:
12-62603400-T-C
gnomAD v4:
12-62603400-T-C
MyVariant Identifiers:
chr12:g.62997180T>C (hg19)
chr12:g.62603400T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.62603400T>C , CM000674.2:g.62603400T>C
GRCh38
NC_000012.11:g.62997180T>C , CM000674.1:g.62997180T>C
GRCh37
NC_000012.10:g.61283447T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_121682.1:n.35A>G
Search 100 bp 5'
Search 100 bp 3'