Canonical Allele Identifier: CA915941652
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 812951
ClinVar RCV Id: RCV001003887

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202541890_202550241del , CM000664.2:g.202541890_202550241del GRCh38
NC_000002.11:g.203406613_203414964del , CM000664.1:g.203406613_203414964del GRCh37
NC_000002.10:g.203114858_203123209del NCBI36
NG_009363.1:g.170564_178915del , LRG_712:g.170564_178915del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.1277-421_1414-2475del
ENST00000638587.1:c.1208-421_1345-2475del
ENST00000374574.2:c.1277-421_1414-2475del
ENST00000374580.8:c.1277-421_1414-2475del
NM_001204.6:c.1277-421_1414-2475del , LRG_712t1:c.1277-421_1414-2475del
XM_011511687.1:c.1277-421_1414-2475del
XM_011511688.1:c.1277-421_1414-2475del
NM_001204.7:c.1277-421_1414-2475del