Canonical Allele Identifier: CA915941493
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 812940
ClinVar RCV Id: RCV001003876

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202462494_202466873del , CM000664.2:g.202462494_202466873del GRCh38
NC_000002.11:g.203327217_203331596del , CM000664.1:g.203327217_203331596del GRCh37
NC_000002.10:g.203035462_203039841del NCBI36
NG_009363.1:g.91168_95547del , LRG_712:g.91168_95547del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.77-2315_248-646del
ENST00000374574.2:c.77-2315_248-646del
ENST00000374580.8:c.77-2315_248-646del
NM_001204.6:c.77-2315_248-646del , LRG_712t1:c.77-2315_248-646del
XM_011511687.1:c.77-2315_248-646del
XM_011511688.1:c.77-2315_248-646del
NM_001204.7:c.77-2315_248-646del