Canonical Allele Identifier: CA337489820
Gene: TTTY10 HGNC NCBI

Linked Data

dbSNP Id: rs9785892
gnomAD v3: Y-20472878-A-C
gnomAD v4: Y-20472878-A-C
MyVariant Identifiers: chrY:g.22634764A>C (hg19) chrY:g.20472878A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20472878A>C , CM000686.2:g.20472878A>C GRCh38
NC_000024.9:g.22634764A>C , CM000686.1:g.22634764A>C GRCh37
NC_000024.8:g.21044152A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_001542.1:n.1064-2897T>G
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