ClinGen Allele Registry
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Canonical Allele Identifier:
CA948920898
Gene: LINC02373
HGNC
NCBI
Linked Data - Sequence & Population
gnomAD v3:
12:69433878 G / A
gnomAD v4:
chr12-69433878-G-A
Linked Data - NCBI & NCI
dbSNP:
10748128
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.69433878G>A , CM000674.2:g.69433878G>A
GRCh38
NC_000012.11:g.69827658G>A , CM000674.1:g.69827658G>A
GRCh37
NC_000012.10:g.68113925G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_945061.1:n.163+2165G>A
Search 100 bp 5'
Search 100 bp 3'