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Canonical Allele Identifier:
CA10842679
Gene: LINC01725
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.83789052G>A
GRCh37
chr1:g.84254735G>A
Linked Data - Sequence & Population
gnomAD v2:
1:84254735 G / A
gnomAD v3:
1:83789052 G / A
gnomAD v4:
chr1-83789052-G-A
Joint Max Group AF
0.96714668 (AFR)
Genomes Max Group AF
0.96714668 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7539409
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.83789052G>A , CM000663.2:g.83789052G>A
GRCh38
NC_000001.10:g.84254735G>A , CM000663.1:g.84254735G>A
GRCh37
NC_000001.9:g.84027323G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_119375.1:n.179-38753C>T
Search 100 bp 5'
Search 100 bp 3'