Canonical Allele Identifier: CA337627615
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs1014947271

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8812555C>A , CM000686.2:g.8812555C>A GRCh38
NC_000024.9:g.8680596C>A , CM000686.1:g.8680596C>A GRCh37
NC_000024.8:g.8740596C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+4791G>T
NR_001548.2:n.37+4791G>T