Canonical Allele Identifier: CA337627617
Gene: TTTY11 HGNC NCBI

Linked Data

dbSNP Id: rs9786707
gnomAD v3: Y-8812620-C-T
gnomAD v4: Y-8812620-C-T
MyVariant Identifiers: chrY:g.8680661C>T (hg19) chrY:g.8812620C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8812620C>T , CM000686.2:g.8812620C>T GRCh38
NC_000024.9:g.8680661C>T , CM000686.1:g.8680661C>T GRCh37
NC_000024.8:g.8740661C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253470.4:n.37+4726G>A
NR_001548.2:n.37+4726G>A
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