ClinGen Allele Registry
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Canonical Allele Identifier:
CA337614959
Gene: TSPY24P
HGNC
NCBI
Linked Data
dbSNP Id:
rs34703625
gnomAD v3:
Y-8280828-G-A
gnomAD v4:
Y-8280828-G-A
MyVariant Identifiers:
chrY:g.8148869G>A (hg19)
chrY:g.8280828G>A (hg38)
JSON-LD
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
Search 100 bp 5'
Search 100 bp 3'