Canonical Allele Identifier: CA337715260
Gene: XGY1 HGNC NCBI

Linked Data

dbSNP Id: rs369632620
gnomAD v3: Y-12500156-C-T
gnomAD v4: Y-12500156-C-T
MyVariant Identifiers: chrY:g.14611950C>T (hg19) chrY:g.12500156C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12500156C>T , CM000686.2:g.12500156C>T GRCh38
NC_000024.9:g.14611950C>T , CM000686.1:g.14611950C>T GRCh37
NC_000024.8:g.13121958C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381172.3:n.61+7153G>A
Search 100 bp 5'
Search 100 bp 3'