Canonical Allele Identifier: CA337345785
Gene: TTTY14 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.19021757G>A
GRCh37 chrY:g.21183643G>A
gnomAD v3:
Y:19021757 G / A
gnomAD v4:
chrY-19021757-G-A
Joint Max Group AF 0.95253853 (EAS)
Genomes Max Group AF 0.95253853 (EAS)
dbSNP:
7067384
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19021757G>A , CM000686.2:g.19021757G>A GRCh38
NC_000024.9:g.21183643G>A , CM000686.1:g.21183643G>A GRCh37
NC_000024.8:g.19643031G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125733.1:n.578+46967C>T
NR_125734.1:n.578+46967C>T
NR_125735.1:n.503+55288C>T
NR_125736.1:n.138+46967C>T
NR_125737.1:n.138+46967C>T
NR_001543.4:n.503+55288C>T
NR_125737.2:n.138+46967C>T
NR_158640.1:n.152+51742C>T
NR_158641.1:n.368+22785C>T
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