Canonical Allele Identifier: CA915941648
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 812821
ClinVar RCV Id: RCV001003695
dbSNP Id: rs1574488501

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202519052_202519053insA , CM000664.2:g.202519052_202519053insA GRCh38
NC_000002.11:g.203383775_203383776insA , CM000664.1:g.203383775_203383776insA GRCh37
NC_000002.10:g.203092020_203092021insA NCBI36
NG_009363.1:g.147726_147727insA , LRG_712:g.147726_147727insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.852_852+1insA MANE Select ENSP00000363708.4:n.852_852+1insA
ENST00000638587.1:c.783_783+1insA ENSP00000491062.1:n.783_783+1insA
ENST00000374574.2:c.852_852+1insA ENSP00000363702.2:n.852_852+1insA
ENST00000374580.8:c.852_852+1insA ENSP00000363708.4:n.852_852+1insA
NM_001204.6:c.852_852+1insA , LRG_712t1:c.852_852+1insA NP_001195.2:n.852_852+1insA
XM_011511687.1:c.852_852+1insA XP_011509989.1:n.852_852+1insA
XM_011511688.1:c.852_852+1insA XP_011509990.1:n.852_852+1insA
NM_001204.7:c.852_852+1insA MANE Select NP_001195.2:n.852_852+1insA