Canonical Allele Identifier: CA1139418981
Gene: TTTY14 HGNC NCBI

Linked Data

dbSNP Id: rs2044605498
gnomAD v3: Y-18935702-C-A
gnomAD v4: Y-18935702-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.18935702C>A , CM000686.2:g.18935702C>A GRCh38
NC_000024.9:g.21097588C>A , CM000686.1:g.21097588C>A GRCh37
NC_000024.8:g.19556976C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125733.1:n.579-2227G>T
NR_125734.1:n.579-58497G>T
NR_125735.1:n.504-58497G>T
NR_125736.1:n.139-23220G>T
NR_125737.1:n.139-2861G>T
NR_001543.4:n.504-2861G>T
NR_125737.2:n.139-2861G>T
NR_158640.1:n.153-58497G>T
NR_158641.1:n.369-2861G>T