Canonical Allele Identifier: CA1139039811
Gene: RBMY2QP HGNC NCBI

Linked Data

gnomAD v3: Y-9981642-G-T
gnomAD v4: Y-9981642-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9981642G>T , CM000686.2:g.9981642G>T GRCh38
NC_000024.9:g.9819251G>T , CM000686.1:g.9819251G>T GRCh37
NC_000024.8:g.10429251G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.1003+7548C>A