Canonical Allele Identifier: CA1139039847
Gene: RBMY2QP HGNC NCBI

Linked Data

gnomAD v3: Y-9981741-T-C
gnomAD v4: Y-9981741-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9981741T>C , CM000686.2:g.9981741T>C GRCh38
NC_000024.9:g.9819350T>C , CM000686.1:g.9819350T>C GRCh37
NC_000024.8:g.10429350T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.1003+7449A>G