Canonical Allele Identifier: CA2470059872
Gene: RBMY2QP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.10029131A= , CM000686.2:g.10029131A= GRCh38
NC_000024.9:g.9866740A= , CM000686.1:g.9866740A= GRCh37
NC_000024.8:g.10476740A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429799.1:n.379+1258T=
ENST00000651645.1:n.525+1258T=