ClinGen Allele Registry
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Canonical Allele Identifier:
CA13930491
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.111568950G>A
GRCh37
chr13:g.112221297G>A
Linked Data - Sequence & Population
gnomAD v2:
13:112221297 G / A
gnomAD v3:
13:111568950 G / A
gnomAD v4:
chr13-111568950-G-A
Joint Max Group AF
0.1258892 (NFE)
Genomes Max Group AF
0.1258892 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7333181
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.111568950G>A , CM000675.2:g.111568950G>A
GRCh38
NC_000013.10:g.112221297G>A , CM000675.1:g.112221297G>A
GRCh37
NC_000013.9:g.111019298G>A
NCBI36
Search 100 bp 5'
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