Canonical Allele Identifier: CA337627607

Gene: TTTY11

Linked Data

• dbSNP Id: rs764109872
• gnomAD v3: Y-8811887-G-A
• gnomAD v4: Y-8811887-G-A
• MyVariant Identifiers: chrY:g.8679928G>A (hg19) ; chrY:g.8811887G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.8811887G>A , CM000686.2:g.8811887G>A	GRCh38
NC_000024.9:g.8679928G>A , CM000686.1:g.8679928G>A	GRCh37
NC_000024.8:g.8739928G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000253470.4:n.37+5459C>T
NR_001548.2:n.37+5459C>T