Canonical Allele Identifier: CA337627715
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs147703813
gnomAD v3: Y-8816775-G-A
gnomAD v4: Y-8816775-G-A
MyVariant Identifiers: chrY:g.8684816G>A (hg19) chrY:g.8816775G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8816775G>A , CM000686.2:g.8816775G>A GRCh38
NC_000024.9:g.8684816G>A , CM000686.1:g.8684816G>A GRCh37
NC_000024.8:g.8744816G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+571C>T
NR_001548.2:n.37+571C>T
Search 100 bp 5'
Search 100 bp 3'