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Canonical Allele Identifier:
CA337741299
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrY:g.13948392T>G
GRCh37
chrY:g.16060272T>G
Linked Data - Sequence & Population
gnomAD v3:
Y:13948392 T / G
gnomAD v4:
chrY-13948392-T-G
Joint Max Group AF
0.00037802 (AFR)
Genomes Max Group AF
0.00037802 (AFR)
Linked Data - NCBI & NCI
dbSNP:
111458377
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.13948392T>G , CM000686.2:g.13948392T>G
GRCh38
NC_000024.9:g.16060272T>G , CM000686.1:g.16060272T>G
GRCh37
NC_000024.8:g.14569666T>G
NCBI36
Search 100 bp 5'
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