Canonical Allele Identifier: CA1321556764
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202552878C= , CM000664.2:g.202552878C= GRCh38
NC_000002.11:g.203417601C= , CM000664.1:g.203417601C= GRCh37
NC_000002.10:g.203125846C= NCBI36
NG_009363.1:g.181552C= , LRG_712:g.181552C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1576C= MANE Select ENSP00000363708.4:p.Gln526=
ENST00000638587.1:c.1507C= ENSP00000491062.1:p.Gln503=
ENST00000374574.2:c.1576C= ENSP00000363702.2:p.Gln526=
ENST00000374580.8:c.1576C= ENSP00000363708.4:p.Gln526=
NM_001204.6:c.1576C= , LRG_712t1:c.1576C= NP_001195.2:p.Gln526=
XM_011511687.1:c.1576C= XP_011509989.1:p.Gln526=
XM_011511688.1:c.1576C= XP_011509990.1:p.Gln526=
NM_001204.7:c.1576C= MANE Select NP_001195.2:p.Gln526=