Canonical Allele Identifier: CA337627715
Gene: TTTY11 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.8816775G>A
GRCh37 chrY:g.8684816G>A
gnomAD v3:
Y:8816775 G / A
gnomAD v4:
chrY-8816775-G-A
Joint Max Group AF 0.00218242 (NFE)
Genomes Max Group AF 0.00218242 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8816775G>A , CM000686.2:g.8816775G>A GRCh38
NC_000024.9:g.8684816G>A , CM000686.1:g.8684816G>A GRCh37
NC_000024.8:g.8744816G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253470.4:n.37+571C>T
NR_001548.2:n.37+571C>T
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