Canonical Allele Identifier: CA1321544819
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530645G= , CM000664.2:g.202530645G= GRCh38
NC_000002.11:g.203395368G= , CM000664.1:g.203395368G= GRCh37
NC_000002.10:g.203103613G= NCBI36
NG_009363.1:g.159319G= , LRG_712:g.159319G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.968-149G= MANE Select ENSP00000363708.4:n.968-149G=
ENST00000638587.1:c.899-149G= ENSP00000491062.1:n.899-149G=
ENST00000374574.2:c.968-149G= ENSP00000363702.2:n.968-149G=
ENST00000374580.8:c.968-149G= ENSP00000363708.4:n.968-149G=
NM_001204.6:c.968-149G= , LRG_712t1:c.968-149G= NP_001195.2:n.968-149G=
XM_011511687.1:c.968-149G= XP_011509989.1:n.968-149G=
XM_011511688.1:c.968-149G= XP_011509990.1:n.968-149G=
NM_001204.7:c.968-149G= MANE Select NP_001195.2:n.968-149G=