Canonical Allele Identifier: CA1139039792
Gene: RBMY2QP HGNC NCBI

Linked Data

gnomAD v3: Y-9981585-A-G
gnomAD v4: Y-9981585-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9981585A>G , CM000686.2:g.9981585A>G GRCh38
NC_000024.9:g.9819194A>G , CM000686.1:g.9819194A>G GRCh37
NC_000024.8:g.10429194A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.1003+7605T>C