Canonical Allele Identifier: CA337627618
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs973467662
MyVariant Identifiers: chrY:g.8680700A>C (hg19) chrY:g.8812659A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8812659A>C , CM000686.2:g.8812659A>C GRCh38
NC_000024.9:g.8680700A>C , CM000686.1:g.8680700A>C GRCh37
NC_000024.8:g.8740700A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+4687T>G
NR_001548.2:n.37+4687T>G
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