Canonical Allele Identifier: CA2739193099
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs2124321063

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8811894T>C , CM000686.2:g.8811894T>C GRCh38
NC_000024.9:g.8679935T>C , CM000686.1:g.8679935T>C GRCh37
NC_000024.8:g.8739935T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+5452A>G
NR_001548.2:n.37+5452A>G