Canonical Allele Identifier: CA1321559397
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202555929C= , CM000664.2:g.202555929C= GRCh38
NC_000002.11:g.203420652C= , CM000664.1:g.203420652C= GRCh37
NC_000002.10:g.203128897C= NCBI36
NG_009363.1:g.184603C= , LRG_712:g.184603C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2264C= MANE Select ENSP00000363708.4:p.Pro755=
ENST00000638587.1:c.2195C= ENSP00000491062.1:n.2195C=
ENST00000374574.2:c.1586+3041C= ENSP00000363702.2:n.1586+3041C=
ENST00000374580.8:c.2264C= ENSP00000363708.4:p.Pro755=
NM_001204.6:c.2264C= , LRG_712t1:c.2264C= NP_001195.2:p.Pro755=
XM_011511687.1:c.2264C= XP_011509989.1:p.Pro755=
XM_011511688.1:c.1586+3041C= XP_011509990.1:n.1586+3041C=
NM_001204.7:c.2264C= MANE Select NP_001195.2:p.Pro755=