Canonical Allele Identifier: CA337627606
Gene: TTTY11 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3853054

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8811802T>G , CM000686.2:g.8811802T>G GRCh38
NC_000024.9:g.8679843T>G , CM000686.1:g.8679843T>G GRCh37
NC_000024.8:g.8739843T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_001548.2:n.37+5544A>C