ClinGen Allele Registry
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Canonical Allele Identifier:
CA337645439
Gene: RBMY2QP
HGNC
NCBI
Linked Data
dbSNP Id:
rs781317368
gnomAD v3:
Y-9981630-A-G
gnomAD v4:
Y-9981630-A-G
MyVariant Identifiers:
chrY:g.9819239A>G (hg19)
chrY:g.9981630A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.9981630A>G , CM000686.2:g.9981630A>G
GRCh38
NC_000024.9:g.9819239A>G , CM000686.1:g.9819239A>G
GRCh37
NC_000024.8:g.10429239A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000651645.1:n.1003+7560T>C
Search 100 bp 5'
Search 100 bp 3'