Canonical Allele Identifier: CA645293853
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 425734
ClinVar RCV Id: RCV000488803
dbSNP Id: rs1553503473

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202466927_202467684delinsGTAAAGTA , CM000664.2:g.202466927_202467684delinsGTAAAGTA GRCh38
NC_000002.11:g.203331650_203332407delinsGTAAAGTA , CM000664.1:g.203331650_203332407delinsGTAAAGTA GRCh37
NC_000002.10:g.203039895_203040652delinsGTAAAGTA NCBI36
NG_009363.1:g.95601_96358delinsGTAAAGTA , LRG_712:g.95601_96358delinsGTAAAGTA

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.248-592_413delinsGTAAAGTA
ENST00000638587.1:c.177-126_344delinsGTAAAGTA
ENST00000374574.2:c.248-592_413delinsGTAAAGTA
ENST00000374580.8:c.248-592_413delinsGTAAAGTA
ENST00000479069.1:n.155-592_320delinsGTAAAGTA
NM_001204.6:c.248-592_413delinsGTAAAGTA , LRG_712t1:c.248-592_413delinsGTAAAGTA
XM_011511687.1:c.248-592_413delinsGTAAAGTA
XM_011511688.1:c.248-592_413delinsGTAAAGTA
NM_001204.7:c.248-592_413delinsGTAAAGTA