ClinGen Allele Registry
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Canonical Allele Identifier:
CA337742814
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.14110721C>T
GRCh37
chrY:g.16222601C>T
Linked Data - Sequence & Population
gnomAD v3:
Y:14110721 C / T
gnomAD v4:
chrY-14110721-C-T
Joint Max Group AF
0.00088782 (AMR)
Genomes Max Group AF
0.00088782 (AMR)
Linked Data - NCBI & NCI
dbSNP:
897050306
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.14110721C>T , CM000686.2:g.14110721C>T
GRCh38
NC_000024.9:g.16222601C>T , CM000686.1:g.16222601C>T
GRCh37
NC_000024.8:g.14731995C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'