Canonical Allele Identifier: CA2470012941
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs1603125017

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8812786T>C , CM000686.2:g.8812786T>C GRCh38
NC_000024.9:g.8680827T>C , CM000686.1:g.8680827T>C GRCh37
NC_000024.8:g.8740827T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253470.4:n.37+4560A>G
NR_001548.2:n.37+4560A>G