Canonical Allele Identifier: CA337334235
Gene: TTTY14 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.18921534T>A
GRCh37 chrY:g.21083420T>A
gnomAD v3:
Y:18921534 T / A
gnomAD v4:
chrY-18921534-T-A
Joint Max Group AF 0.63054519 (AFR)
Genomes Max Group AF 0.63054519 (AFR)
dbSNP:
16980577
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.18921534T>A , CM000686.2:g.18921534T>A GRCh38
NC_000024.9:g.21083420T>A , CM000686.1:g.21083420T>A GRCh37
NC_000024.8:g.19542808T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125733.1:n.796+11209A>T
NR_125734.1:n.579-44329A>T
NR_125735.1:n.504-44329A>T
NR_125736.1:n.139-9052A>T
NR_158640.1:n.153-44329A>T
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