ClinGen Allele Registry
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Canonical Allele Identifier:
CA1691423503
Gene: LINC02889
HGNC
NCBI
Linked Data - NCBI & NCI
dbSNP:
10499504
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.17521959A>C , CM000669.2:g.17521959A>C
GRCh38
NC_000007.13:g.17561583A>C , CM000669.1:g.17561583A>C
GRCh37
NC_000007.12:g.17528108A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110013.1:n.158+36793T>G
Search 100 bp 5'
Search 100 bp 3'