Canonical Allele Identifier: CA1138972631
Gene: TTTY11 HGNC NCBI

Linked Data

gnomAD v3: Y-8812687-C-A
gnomAD v4: Y-8812687-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8812687C>A , CM000686.2:g.8812687C>A GRCh38
NC_000024.9:g.8680728C>A , CM000686.1:g.8680728C>A GRCh37
NC_000024.8:g.8740728C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+4659G>T
NR_001548.2:n.37+4659G>T