ClinGen Allele Registry
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Canonical Allele Identifier:
CA337765574
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.15183078C>T
GRCh37
chrY:g.17294958C>T
Linked Data - Sequence & Population
gnomAD v3:
Y:15183078 C / T
gnomAD v4:
chrY-15183078-C-T
Joint Max Group AF
0.18980521 (AFR)
Genomes Max Group AF
0.18980521 (AFR)
Linked Data - NCBI & NCI
dbSNP:
16980502
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.15183078C>T , CM000686.2:g.15183078C>T
GRCh38
NC_000024.9:g.17294958C>T , CM000686.1:g.17294958C>T
GRCh37
NC_000024.8:g.15804352C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'