ClinGen Allele Registry
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Canonical Allele Identifier:
CA11388149
Gene: LINC02015
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.177879201G>A
GRCh37
chr3:g.177596989G>A
Linked Data - Sequence & Population
gnomAD v2:
3:177596989 G / A
gnomAD v3:
3:177879201 G / A
gnomAD v4:
chr3-177879201-G-A
Joint Max Group AF
0.6436501 (NFE)
Genomes Max Group AF
0.6436501 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7612209
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.177879201G>A , CM000665.2:g.177879201G>A
GRCh38
NC_000003.11:g.177596989G>A , CM000665.1:g.177596989G>A
GRCh37
NC_000003.10:g.179079683G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110826.1:n.133-16412G>A
Search 100 bp 5'
Search 100 bp 3'