ClinGen Allele Registry
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Canonical Allele Identifier:
CA337645432
Gene: RBMY2QP
HGNC
NCBI
Linked Data
dbSNP Id:
rs13305766
MyVariant Identifiers:
chrY:g.9819185A>T (hg19)
chrY:g.9981576A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.9981576A>T , CM000686.2:g.9981576A>T
GRCh38
NC_000024.9:g.9819185A>T , CM000686.1:g.9819185A>T
GRCh37
NC_000024.8:g.10429185A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000651645.1:n.1003+7614T>A
Search 100 bp 5'
Search 100 bp 3'