Canonical Allele Identifier: CA1321559628
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556084A= , CM000664.2:g.202556084A= GRCh38
NC_000002.11:g.203420807A= , CM000664.1:g.203420807A= GRCh37
NC_000002.10:g.203129052A= NCBI36
NG_009363.1:g.184758A= , LRG_712:g.184758A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2419A= MANE Select ENSP00000363708.4:p.Asn807=
ENST00000638587.1:c.2350A= ENSP00000491062.1:n.2350A=
ENST00000374574.2:c.1586+3196A= ENSP00000363702.2:n.1586+3196A=
ENST00000374580.8:c.2419A= ENSP00000363708.4:p.Asn807=
NM_001204.6:c.2419A= , LRG_712t1:c.2419A= NP_001195.2:p.Asn807=
XM_011511687.1:c.2419A= XP_011509989.1:p.Asn807=
XM_011511688.1:c.1586+3196A= XP_011509990.1:n.1586+3196A=
NM_001204.7:c.2419A= MANE Select NP_001195.2:p.Asn807=