Canonical Allele Identifier: CA337627722
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs4141564
gnomAD v3: Y-8817042-G-A
gnomAD v4: Y-8817042-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8817042G>A , CM000686.2:g.8817042G>A GRCh38
NC_000024.9:g.8685083G>A , CM000686.1:g.8685083G>A GRCh37
NC_000024.8:g.8745083G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+304C>T
NR_001548.2:n.37+304C>T