Canonical Allele Identifier: CA337614959
Gene: TSPY24P HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.8280828G>A
GRCh37 chrY:g.8148869G>A
gnomAD v3:
Y:8280828 G / A
gnomAD v4:
chrY-8280828-G-A
Joint Max Group AF 0.10352247 (AMR)
Genomes Max Group AF 0.10352247 (AMR)
dbSNP:
34703625
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8280828G>A , CM000686.2:g.8280828G>A GRCh38
NC_000024.9:g.8148869G>A , CM000686.1:g.8148869G>A GRCh37
NC_000024.8:g.8208869G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000431340.1:n.138+493G>A
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