Canonical Allele Identifier: CA337614980
Gene: TSPY24P HGNC NCBI
dbSNP:
9786882
gnomAD v3:
Y:8281307 G / A
gnomAD v4:
chrY-8281307-G-A
Joint Max Group AF 0.95097408 (EAS)
Genomes Max Group AF 0.95097408 (EAS)
MyVariant.info:
GRCh38 chrY:g.8281307G>A
GRCh37 chrY:g.8149348G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8281307G>A , CM000686.2:g.8281307G>A GRCh38
NC_000024.9:g.8149348G>A , CM000686.1:g.8149348G>A GRCh37
NC_000024.8:g.8209348G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000431340.1:n.139-394G>A
Search 100 bp 5'
Search 100 bp 3'