Canonical Allele Identifier: CA337768402
Gene:

Linked Data

dbSNP Id: rs35141399
gnomAD v3: Y-15311440-C-T
gnomAD v4: Y-15311440-C-T
MyVariant Identifiers: chrY:g.17423320C>T (hg19) chrY:g.15311440C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15311440C>T , CM000686.2:g.15311440C>T GRCh38
NC_000024.9:g.17423320C>T , CM000686.1:g.17423320C>T GRCh37
NC_000024.8:g.15932714C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001756089.1:n.309+37229G>A
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