Canonical Allele Identifier: CA2589282257
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs2124321070
gnomAD v3: Y-8811945-C-T
gnomAD v4: Y-8811945-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8811945C>T , CM000686.2:g.8811945C>T GRCh38
NC_000024.9:g.8679986C>T , CM000686.1:g.8679986C>T GRCh37
NC_000024.8:g.8739986C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+5401G>A
NR_001548.2:n.37+5401G>A