Canonical Allele Identifier: CA645293981
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 425944
ClinVar RCV Id: RCV000488514
dbSNP Id: rs1085307353
MyVariant Identifiers: chr2:g.203417452del (hg19) chr2:g.202552729del (hg38)
PubMed: PMID:11115378 PMID:16429395 PMID:26387786
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202552729del , CM000664.2:g.202552729del GRCh38
NC_000002.11:g.203417452del , CM000664.1:g.203417452del GRCh37
NC_000002.10:g.203125697del NCBI36
NG_009363.1:g.181403del , LRG_712:g.181403del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.1427del MANE Select ENSP00000363708.4:p.Leu476ProfsTer30
ENST00000638587.1:c.1358del ENSP00000491062.1:p.Leu453ProfsTer30
ENST00000374574.2:c.1427del ENSP00000363702.2:p.Leu476ProfsTer30
ENST00000374580.8:c.1427del ENSP00000363708.4:p.Leu476ProfsTer30
NM_001204.6:c.1427del , LRG_712t1:c.1427del NP_001195.2:p.Leu476ProfsTer30
XM_011511687.1:c.1427del XP_011509989.1:p.Leu476ProfsTer30
XM_011511688.1:c.1427del XP_011509990.1:p.Leu476ProfsTer30
NM_001204.7:c.1427del MANE Select NP_001195.2:p.Leu476ProfsTer30
Search 100 bp 5'
Search 100 bp 3'