ClinGen Allele Registry
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Canonical Allele Identifier:
CA337748392
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.14366672A>G
GRCh37
chrY:g.16478552A>G
Linked Data - Sequence & Population
gnomAD v3:
Y:14366672 A / G
gnomAD v4:
chrY-14366672-A-G
Joint Max Group AF
0.21986285 (AFR)
Genomes Max Group AF
0.21986285 (AFR)
Linked Data - NCBI & NCI
dbSNP:
16980370
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.14366672A>G , CM000686.2:g.14366672A>G
GRCh38
NC_000024.9:g.16478552A>G , CM000686.1:g.16478552A>G
GRCh37
NC_000024.8:g.14987946A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'