Canonical Allele Identifier: CA337627722
Gene: TTTY11 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.8817042G>A
GRCh37 chrY:g.8685083G>A
gnomAD v3:
Y:8817042 G / A
gnomAD v4:
chrY-8817042-G-A
Joint Max Group AF 0.93273513 (EAS)
Genomes Max Group AF 0.93273513 (EAS)
dbSNP:
4141564
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8817042G>A , CM000686.2:g.8817042G>A GRCh38
NC_000024.9:g.8685083G>A , CM000686.1:g.8685083G>A GRCh37
NC_000024.8:g.8745083G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253470.4:n.37+304C>T
NR_001548.2:n.37+304C>T
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