Canonical Allele Identifier: CA1321545659
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202532627G= , CM000664.2:g.202532627G= GRCh38
NC_000002.11:g.203397350G= , CM000664.1:g.203397350G= GRCh37
NC_000002.10:g.203105595G= NCBI36
NG_009363.1:g.161301G= , LRG_712:g.161301G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1171G= MANE Select ENSP00000363708.4:p.Ala391=
ENST00000638587.1:c.1102G= ENSP00000491062.1:p.Ala368=
ENST00000374574.2:c.1171G= ENSP00000363702.2:p.Ala391=
ENST00000374580.8:c.1171G= ENSP00000363708.4:p.Ala391=
NM_001204.6:c.1171G= , LRG_712t1:c.1171G= NP_001195.2:p.Ala391=
XM_011511687.1:c.1171G= XP_011509989.1:p.Ala391=
XM_011511688.1:c.1171G= XP_011509990.1:p.Ala391=
NM_001204.7:c.1171G= MANE Select NP_001195.2:p.Ala391=