Canonical Allele Identifier: CA1139440098
Gene: TTTY14 HGNC NCBI

Linked Data

dbSNP Id: rs2044677665
gnomAD v3: Y-18997253-A-G
gnomAD v4: Y-18997253-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.18997253A>G , CM000686.2:g.18997253A>G GRCh38
NC_000024.9:g.21159139A>G , CM000686.1:g.21159139A>G GRCh37
NC_000024.8:g.19618527A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125733.1:n.579-63778T>C
NR_125734.1:n.578+71471T>C
NR_125735.1:n.503+79792T>C
NR_125736.1:n.138+71471T>C
NR_125737.1:n.139-64412T>C
NR_001543.4:n.504-64412T>C
NR_125737.2:n.139-64412T>C
NR_158640.1:n.152+76246T>C
NR_158641.1:n.368+47289T>C