Canonical Allele Identifier: CA1321507706
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202464918A= , CM000664.2:g.202464918A= GRCh38
NC_000002.11:g.203329641A= , CM000664.1:g.203329641A= GRCh37
NC_000002.10:g.203037886A= NCBI36
NG_009363.1:g.93592A= , LRG_712:g.93592A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.186A= MANE Select ENSP00000363708.4:p.Lys62=
ENST00000638587.1:c.111A= ENSP00000491062.1:p.Lys37=
ENST00000374574.2:c.186A= ENSP00000363702.2:p.Lys62=
ENST00000374580.8:c.186A= ENSP00000363708.4:p.Lys62=
ENST00000479069.1:n.93A=
NM_001204.6:c.186A= , LRG_712t1:c.186A= NP_001195.2:p.Lys62=
XM_011511687.1:c.186A= XP_011509989.1:p.Lys62=
XM_011511688.1:c.186A= XP_011509990.1:p.Lys62=
NM_001204.7:c.186A= MANE Select NP_001195.2:p.Lys62=