Canonical Allele Identifier: CA337715102
Gene: XGY1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12484660C>T
GRCh37 chrY:g.14596460C>T
gnomAD v3:
Y:12484660 C / T
gnomAD v4:
chrY-12484660-C-T
Joint Max Group AF 0.14329394 (NFE)
Genomes Max Group AF 0.11050926 (NFE)
Exomes Max Group AF 0.14676002 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12484660C>T , CM000686.2:g.12484660C>T GRCh38
NC_000024.9:g.14596460C>T , CM000686.1:g.14596460C>T GRCh37
NC_000024.8:g.13106468C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381172.3:n.121+71G>A
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