Canonical Allele Identifier: CA1321507501
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202464824A= , CM000664.2:g.202464824A= GRCh38
NC_000002.11:g.203329547A= , CM000664.1:g.203329547A= GRCh37
NC_000002.10:g.203037792A= NCBI36
NG_009363.1:g.93498A= , LRG_712:g.93498A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.92A= MANE Select ENSP00000363708.4:p.Glu31=
ENST00000638587.1:c.17A= ENSP00000491062.1:p.Glu6=
ENST00000374574.2:c.92A= ENSP00000363702.2:p.Glu31=
ENST00000374580.8:c.92A= ENSP00000363708.4:p.Glu31=
NM_001204.6:c.92A= , LRG_712t1:c.92A= NP_001195.2:p.Glu31=
XM_011511687.1:c.92A= XP_011509989.1:p.Glu31=
XM_011511688.1:c.92A= XP_011509990.1:p.Glu31=
NM_001204.7:c.92A= MANE Select NP_001195.2:p.Glu31=