Canonical Allele Identifier: CA337627616
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs866252181

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8812608A>G , CM000686.2:g.8812608A>G GRCh38
NC_000024.9:g.8680649A>G , CM000686.1:g.8680649A>G GRCh37
NC_000024.8:g.8740649A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+4738T>C
NR_001548.2:n.37+4738T>C