ClinGen Allele Registry
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Canonical Allele Identifier:
CA13891119
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr13:g.103317141G>A
GRCh37
chr13:g.103969491G>A
Linked Data - Sequence & Population
gnomAD v2:
13:103969491 G / A
gnomAD v3:
13:103317141 G / A
gnomAD v4:
chr13-103317141-G-A
Joint Max Group AF
0.71411592 (AFR)
Genomes Max Group AF
0.71411592 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4771450
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.103317141G>A , CM000675.2:g.103317141G>A
GRCh38
NC_000013.10:g.103969491G>A , CM000675.1:g.103969491G>A
GRCh37
NC_000013.9:g.102767492G>A
NCBI36
Search 100 bp 5'
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