ClinGen Allele Registry
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Canonical Allele Identifier:
CA337296582
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.17237735T>C
GRCh37
chrY:g.19349615T>C
Linked Data - Sequence & Population
gnomAD v3:
Y:17237735 T / C
gnomAD v4:
chrY-17237735-T-C
Joint Max Group AF
0.69842936 (AFR)
Genomes Max Group AF
0.69842936 (AFR)
Linked Data - NCBI & NCI
dbSNP:
16980396
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.17237735T>C , CM000686.2:g.17237735T>C
GRCh38
NC_000024.9:g.19349615T>C , CM000686.1:g.19349615T>C
GRCh37
NC_000024.8:g.17859009T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'