Canonical Allele Identifier: CA337645946
Gene: RBMY2QP HGNC NCBI

Linked Data

dbSNP Id: rs34907718

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9993950T>G , CM000686.2:g.9993950T>G GRCh38
NC_000024.9:g.9831559T>G , CM000686.1:g.9831559T>G GRCh37
NC_000024.8:g.10441559T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651645.1:n.953+1647A>C