Canonical Allele Identifier: CA337646107
Gene: RBMY2QP HGNC NCBI

Linked Data

dbSNP Id: rs9645182
MyVariant Identifiers: chrY:g.9836911T>G (hg19) chrY:g.9999302T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9999302T>G , CM000686.2:g.9999302T>G GRCh38
NC_000024.9:g.9836911T>G , CM000686.1:g.9836911T>G GRCh37
NC_000024.8:g.10446911T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651645.1:n.835-3587A>C
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