Canonical Allele Identifier: CA1138972369
Gene: TTTY11 HGNC NCBI

Linked Data

gnomAD v3: Y-8811891-C-G
gnomAD v4: Y-8811891-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8811891C>G , CM000686.2:g.8811891C>G GRCh38
NC_000024.9:g.8679932C>G , CM000686.1:g.8679932C>G GRCh37
NC_000024.8:g.8739932C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+5455G>C
NR_001548.2:n.37+5455G>C