ClinGen Allele Registry
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Canonical Allele Identifier:
CA761543497
Gene: LINC01934
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.181131318A>C
GRCh37
chr2:g.181996045A>C
Linked Data - NCBI & NCI
dbSNP:
13010713
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.181131318A>C , CM000664.2:g.181131318A>C
GRCh38
NC_000002.11:g.181996045A>C , CM000664.1:g.181996045A>C
GRCh37
NC_000002.10:g.181704290A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_130784.1:n.144+7338A>C
Search 100 bp 5'
Search 100 bp 3'