ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA337714686
Gene: XGY1
HGNC
NCBI
Linked Data
dbSNP Id:
rs111515425
gnomAD v3:
Y-12444629-G-A
gnomAD v4:
Y-12444629-G-A
MyVariant Identifiers:
chrY:g.14556428G>A (hg19)
chrY:g.12444629G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.12444629G>A , CM000686.2:g.12444629G>A
GRCh38
NC_000024.9:g.14556428G>A , CM000686.1:g.14556428G>A
GRCh37
NC_000024.8:g.13066436G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000381172.3:n.294-1329C>T
Search 100 bp 5'
Search 100 bp 3'