Canonical Allele Identifier: CA1139039788
Gene: RBMY2QP HGNC NCBI

Linked Data

dbSNP Id: rs2016373375
gnomAD v3: Y-9981557-TA-T
gnomAD v4: Y-9981557-TA-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9981559del , CM000686.2:g.9981559del GRCh38
NC_000024.9:g.9819168del , CM000686.1:g.9819168del GRCh37
NC_000024.8:g.10429168del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.1003+7632del