Canonical Allele Identifier: CA337627608

Gene: TTTY11

Linked Data

• dbSNP Id: rs199987612
• gnomAD v3: Y-8811913-T-C
• gnomAD v4: Y-8811913-T-C
• MyVariant Identifiers: chrY:g.8679954T>C (hg19) ; chrY:g.8811913T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.8811913T>C , CM000686.2:g.8811913T>C	GRCh38
NC_000024.9:g.8679954T>C , CM000686.1:g.8679954T>C	GRCh37
NC_000024.8:g.8739954T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000253470.4:n.37+5433A>G
NR_001548.2:n.37+5433A>G