Canonical Allele Identifier: CA2824584630
Gene: RBMY2QP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9994021G>T , CM000686.2:g.9994021G>T GRCh38
NC_000024.9:g.9831630G>T , CM000686.1:g.9831630G>T GRCh37
NC_000024.8:g.10441630G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.953+1576C>A