Canonical Allele Identifier: CA337715261
Gene: XGY1 HGNC NCBI

Linked Data

dbSNP Id: rs111696152
gnomAD v3: Y-12500272-C-A
gnomAD v4: Y-12500272-C-A
MyVariant Identifiers: chrY:g.14612066C>A (hg19) chrY:g.12500272C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12500272C>A , CM000686.2:g.12500272C>A GRCh38
NC_000024.9:g.14612066C>A , CM000686.1:g.14612066C>A GRCh37
NC_000024.8:g.13122074C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381172.3:n.61+7037G>T
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