Canonical Allele Identifier: CA1138972407
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs2015542628
gnomAD v3: Y-8811942-G-C
gnomAD v4: Y-8811942-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8811942G>C , CM000686.2:g.8811942G>C GRCh38
NC_000024.9:g.8679983G>C , CM000686.1:g.8679983G>C GRCh37
NC_000024.8:g.8739983G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253470.4:n.37+5404C>G
NR_001548.2:n.37+5404C>G