Canonical Allele Identifier: CA915941492
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 812939
ClinVar RCV Id: RCV001003875

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202461237_202467808del , CM000664.2:g.202461237_202467808del GRCh38
NC_000002.11:g.203325960_203332531del , CM000664.1:g.203325960_203332531del GRCh37
NC_000002.10:g.203034205_203040776del NCBI36
NG_009363.1:g.89911_96482del , LRG_712:g.89911_96482del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.77-3572_418+119del
ENST00000374574.2:c.77-3572_418+119del
ENST00000374580.8:c.77-3572_418+119del
NM_001204.6:c.77-3572_418+119del , LRG_712t1:c.77-3572_418+119del
XM_011511687.1:c.77-3572_418+119del
XM_011511688.1:c.77-3572_418+119del
NM_001204.7:c.77-3572_418+119del