ClinGen Allele Registry
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Canonical Allele Identifier:
CA337575936
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.7127482A>G
GRCh37
chrY:g.6995523A>G
Linked Data - Sequence & Population
gnomAD v3:
Y:7127482 A / G
gnomAD v4:
chrY-7127482-A-G
Joint Max Group AF
0.66300534 (AFR)
Genomes Max Group AF
0.66300534 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7893107
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.7127482A>G , CM000686.2:g.7127482A>G
GRCh38
NC_000024.9:g.6995523A>G , CM000686.1:g.6995523A>G
GRCh37
NC_000024.8:g.7055523A>G
NCBI36
Search 100 bp 5'
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