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Canonical Allele Identifier:
CA13649454
Gene: LINC02373
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.69434901G>A
GRCh37
chr12:g.69828681G>A
Linked Data - Sequence & Population
gnomAD v2:
12:69828681 G / A
gnomAD v3:
12:69434901 G / A
gnomAD v4:
chr12-69434901-G-A
Joint Max Group AF
0.33622973 (SAS)
Genomes Max Group AF
0.33622973 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11177669
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.69434901G>A , CM000674.2:g.69434901G>A
GRCh38
NC_000012.11:g.69828681G>A , CM000674.1:g.69828681G>A
GRCh37
NC_000012.10:g.68114948G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_945061.1:n.163+3188G>A
Search 100 bp 5'
Search 100 bp 3'