ClinGen Allele Registry
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Canonical Allele Identifier:
CA337707817
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.12078626C>T
GRCh37
chrY:g.14199332C>T
Linked Data - Sequence & Population
gnomAD v3:
Y:12078626 C / T
gnomAD v4:
chrY-12078626-C-T
Joint Max Group AF
0.00132451 (AMR)
Genomes Max Group AF
0.00132451 (AMR)
Linked Data - NCBI & NCI
dbSNP:
955722212
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.12078626C>T , CM000686.2:g.12078626C>T
GRCh38
NC_000024.9:g.14199332C>T , CM000686.1:g.14199332C>T
GRCh37
NC_000024.8:g.12709332C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'