Canonical Allele Identifier: CA337646546
Gene: RBMY2QP HGNC NCBI

Linked Data

dbSNP Id: rs9786489
gnomAD v3: Y-10013848-G-T
gnomAD v4: Y-10013848-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.10013848G>T , CM000686.2:g.10013848G>T GRCh38
NC_000024.9:g.9851457G>T , CM000686.1:g.9851457G>T GRCh37
NC_000024.8:g.10461457G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.834+9347C>A