Canonical Allele Identifier: CA880361072
Gene: TTTY14 HGNC NCBI

Linked Data

dbSNP Id: rs1218244383

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.18935541A>T , CM000686.2:g.18935541A>T GRCh38
NC_000024.9:g.21097427A>T , CM000686.1:g.21097427A>T GRCh37
NC_000024.8:g.19556815A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125733.1:n.579-2066T>A
NR_125734.1:n.579-58336T>A
NR_125735.1:n.504-58336T>A
NR_125736.1:n.139-23059T>A
NR_125737.1:n.139-2700T>A
NR_001543.4:n.504-2700T>A
NR_125737.2:n.139-2700T>A
NR_158640.1:n.153-58336T>A
NR_158641.1:n.369-2700T>A