Canonical Allele Identifier: CA915941649
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 812947
ClinVar RCV Id: RCV001003883

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202519368_202523159del , CM000664.2:g.202519368_202523159del GRCh38
NC_000002.11:g.203384091_203387882del , CM000664.1:g.203384091_203387882del GRCh37
NC_000002.10:g.203092336_203096127del NCBI36
NG_009363.1:g.148042_151833del , LRG_712:g.148042_151833del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.852+316_967+2958del
ENST00000638587.1:c.783+316_898+2958del
ENST00000374574.2:c.852+316_967+2958del
ENST00000374580.8:c.852+316_967+2958del
NM_001204.6:c.852+316_967+2958del , LRG_712t1:c.852+316_967+2958del
XM_011511687.1:c.852+316_967+2958del
XM_011511688.1:c.852+316_967+2958del
NM_001204.7:c.852+316_967+2958del