Canonical Allele Identifier: CA1139039805
Gene: RBMY2QP HGNC NCBI

Linked Data

dbSNP Id: rs2016373462
gnomAD v3: Y-9981617-G-A
gnomAD v4: Y-9981617-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9981617G>A , CM000686.2:g.9981617G>A GRCh38
NC_000024.9:g.9819226G>A , CM000686.1:g.9819226G>A GRCh37
NC_000024.8:g.10429226G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.1003+7573C>T