Canonical Allele Identifier: CA1138972412
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs1603124992
gnomAD v3: Y-8811960-T-A
gnomAD v4: Y-8811960-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8811960T>A , CM000686.2:g.8811960T>A GRCh38
NC_000024.9:g.8680001T>A , CM000686.1:g.8680001T>A GRCh37
NC_000024.8:g.8740001T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+5386A>T
NR_001548.2:n.37+5386A>T
Search 100 bp 5'
Search 100 bp 3'