Canonical Allele Identifier: CA1321550601
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202542329A= , CM000664.2:g.202542329A= GRCh38
NC_000002.11:g.203407052A= , CM000664.1:g.203407052A= GRCh37
NC_000002.10:g.203115297A= NCBI36
NG_009363.1:g.171003A= , LRG_712:g.171003A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1295A= MANE Select ENSP00000363708.4:p.Tyr432=
ENST00000638587.1:c.1226A= ENSP00000491062.1:p.Tyr409=
ENST00000374574.2:c.1295A= ENSP00000363702.2:p.Tyr432=
ENST00000374580.8:c.1295A= ENSP00000363708.4:p.Tyr432=
NM_001204.6:c.1295A= , LRG_712t1:c.1295A= NP_001195.2:p.Tyr432=
XM_011511687.1:c.1295A= XP_011509989.1:p.Tyr432=
XM_011511688.1:c.1295A= XP_011509990.1:p.Tyr432=
NM_001204.7:c.1295A= MANE Select NP_001195.2:p.Tyr432=