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Canonical Allele Identifier:
CA301355850
Gene: LINC02565
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr18:g.57316323G>T
GRCh37
chr18:g.54983554G>T
Linked Data - Sequence & Population
gnomAD v2:
18:54983554 G / T
gnomAD v3:
18:57316323 G / T
gnomAD v4:
chr18-57316323-G-T
Joint Max Group AF
0.43506177 (AFR)
Genomes Max Group AF
0.43506177 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1120787
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.57316323G>T , CM000680.2:g.57316323G>T
GRCh38
NC_000018.9:g.54983554G>T , CM000680.1:g.54983554G>T
GRCh37
NC_000018.8:g.53134552G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_935518.1:n.203+17807C>A
Search 100 bp 5'
Search 100 bp 3'