Canonical Allele Identifier: CA1139042957
Gene: RBMY2QP HGNC NCBI

Linked Data

dbSNP Id: rs2016384263

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9993985_9993986dup , CM000686.2:g.9993985_9993986dup GRCh38
NC_000024.9:g.9831594_9831595dup , CM000686.1:g.9831594_9831595dup GRCh37
NC_000024.8:g.10441594_10441595dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.953+1627_953+1628dup