ClinGen Allele Registry
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Canonical Allele Identifier:
CA1180186316
Gene: LINC01725
HGNC
NCBI
Linked Data - NCBI & NCI
dbSNP:
7539409
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.83789052G>C , CM000663.2:g.83789052G>C
GRCh38
NC_000001.10:g.84254735G>C , CM000663.1:g.84254735G>C
GRCh37
NC_000001.9:g.84027323G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_119375.1:n.179-38753C>G
Search 100 bp 5'
Search 100 bp 3'