ClinGen Allele Registry
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Canonical Allele Identifier:
CA13192239
Gene: LINC02621
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.62277122G>C , CM000672.2:g.62277122G>C
GRCh38
NC_000010.10:g.64036881G>C , CM000672.1:g.64036881G>C
GRCh37
NC_000010.9:g.63706887G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_945999.1:n.125-25204G>C
Search 100 bp 5'
Search 100 bp 3'