Canonical Allele Identifier: CA1139043019
Gene: RBMY2QP HGNC NCBI

Linked Data

gnomAD v3: Y-9994040-C-G
gnomAD v4: Y-9994040-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9994040C>G , CM000686.2:g.9994040C>G GRCh38
NC_000024.9:g.9831649C>G , CM000686.1:g.9831649C>G GRCh37
NC_000024.8:g.10441649C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.953+1557G>C