Canonical Allele Identifier: CA337742813
Gene:
MyVariant.info:
GRCh38 chrY:g.14110681T>C
GRCh37 chrY:g.16222561T>C
gnomAD v3:
Y:14110681 T / C
gnomAD v4:
chrY-14110681-T-C
Joint Max Group AF 0.93485962 (EAS)
Genomes Max Group AF 0.93485962 (EAS)
dbSNP:
9785994
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14110681T>C , CM000686.2:g.14110681T>C GRCh38
NC_000024.9:g.16222561T>C , CM000686.1:g.16222561T>C GRCh37
NC_000024.8:g.14731955T>C NCBI36
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