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Canonical Allele Identifier:
CA13592967
Gene: LINC02373
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.69433878G>T
GRCh37
chr12:g.69827658G>T
Linked Data - Sequence & Population
gnomAD v2:
12:69827658 G / T
gnomAD v3:
12:69433878 G / T
gnomAD v4:
chr12-69433878-G-T
Joint Max Group AF
0.63427092 (EAS)
Genomes Max Group AF
0.63427092 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10748128
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.69433878G>T , CM000674.2:g.69433878G>T
GRCh38
NC_000012.11:g.69827658G>T , CM000674.1:g.69827658G>T
GRCh37
NC_000012.10:g.68113925G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_945061.1:n.163+2165G>T
Search 100 bp 5'
Search 100 bp 3'