Canonical Allele Identifier: CA1321544817
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530643A= , CM000664.2:g.202530643A= GRCh38
NC_000002.11:g.203395366A= , CM000664.1:g.203395366A= GRCh37
NC_000002.10:g.203103611A= NCBI36
NG_009363.1:g.159317A= , LRG_712:g.159317A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.968-151A= MANE Select ENSP00000363708.4:n.968-151A=
ENST00000638587.1:c.899-151A= ENSP00000491062.1:n.899-151A=
ENST00000374574.2:c.968-151A= ENSP00000363702.2:n.968-151A=
ENST00000374580.8:c.968-151A= ENSP00000363708.4:n.968-151A=
NM_001204.6:c.968-151A= , LRG_712t1:c.968-151A= NP_001195.2:n.968-151A=
XM_011511687.1:c.968-151A= XP_011509989.1:n.968-151A=
XM_011511688.1:c.968-151A= XP_011509990.1:n.968-151A=
NM_001204.7:c.968-151A= MANE Select NP_001195.2:n.968-151A=