Canonical Allele Identifier: CA2470057467
Gene: RBMY2QP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9981596A= , CM000686.2:g.9981596A= GRCh38
NC_000024.9:g.9819205A= , CM000686.1:g.9819205A= GRCh37
NC_000024.8:g.10429205A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.1003+7594T=