Canonical Allele Identifier: CA350399333
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 425711
ClinVar RCV Id: RCV000488815
dbSNP Id: rs1085307171

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202464910T>G , CM000664.2:g.202464910T>G GRCh38
NC_000002.11:g.203329633T>G , CM000664.1:g.203329633T>G GRCh37
NC_000002.10:g.203037878T>G NCBI36
NG_009363.1:g.93584T>G , LRG_712:g.93584T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.178T>G MANE Select ENSP00000363708.4:p.Cys60Gly
ENST00000638587.1:c.103T>G ENSP00000491062.1:p.Cys35Gly
ENST00000374574.2:c.178T>G ENSP00000363702.2:p.Cys60Gly
ENST00000374580.8:c.178T>G ENSP00000363708.4:p.Cys60Gly
ENST00000479069.1:n.85T>G
NM_001204.6:c.178T>G , LRG_712t1:c.178T>G NP_001195.2:p.Cys60Gly
XM_011511687.1:c.178T>G XP_011509989.1:p.Cys60Gly
XM_011511688.1:c.178T>G XP_011509990.1:p.Cys60Gly
NM_001204.7:c.178T>G MANE Select NP_001195.2:p.Cys60Gly