Canonical Allele Identifier: CA2470058077
Gene: RBMY2QP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9993968T= , CM000686.2:g.9993968T= GRCh38
NC_000024.9:g.9831577T= , CM000686.1:g.9831577T= GRCh37
NC_000024.8:g.10441577T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.953+1629A=