Canonical Allele Identifier: CA1321539807
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202519179T= , CM000664.2:g.202519179T= GRCh38
NC_000002.11:g.203383902T= , CM000664.1:g.203383902T= GRCh37
NC_000002.10:g.203092147T= NCBI36
NG_009363.1:g.147853T= , LRG_712:g.147853T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.852+127T= MANE Select ENSP00000363708.4:n.852+127T=
ENST00000638587.1:c.783+127T= ENSP00000491062.1:n.783+127T=
ENST00000374574.2:c.852+127T= ENSP00000363702.2:n.852+127T=
ENST00000374580.8:c.852+127T= ENSP00000363708.4:n.852+127T=
NM_001204.6:c.852+127T= , LRG_712t1:c.852+127T= NP_001195.2:n.852+127T=
XM_011511687.1:c.852+127T= XP_011509989.1:n.852+127T=
XM_011511688.1:c.852+127T= XP_011509990.1:n.852+127T=
NM_001204.7:c.852+127T= MANE Select NP_001195.2:n.852+127T=