ClinGen Allele Registry
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Canonical Allele Identifier:
CA1230642205
Gene: LINC02774
HGNC
NCBI
Linked Data - NCBI & NCI
dbSNP:
476141
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.244013122G>C , CM000663.2:g.244013122G>C
GRCh38
NC_000001.10:g.244176424G>C , CM000663.1:g.244176424G>C
GRCh37
NC_000001.9:g.242243047G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_033883.1:n.750+2202G>C
Search 100 bp 5'
Search 100 bp 3'