Canonical Allele Identifier: CA1321559393
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202555926G= , CM000664.2:g.202555926G= GRCh38
NC_000002.11:g.203420649G= , CM000664.1:g.203420649G= GRCh37
NC_000002.10:g.203128894G= NCBI36
NG_009363.1:g.184600G= , LRG_712:g.184600G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2261G= MANE Select ENSP00000363708.4:p.Arg754=
ENST00000638587.1:c.2192G= ENSP00000491062.1:n.2192G=
ENST00000374574.2:c.1586+3038G= ENSP00000363702.2:n.1586+3038G=
ENST00000374580.8:c.2261G= ENSP00000363708.4:p.Arg754=
NM_001204.6:c.2261G= , LRG_712t1:c.2261G= NP_001195.2:p.Arg754=
XM_011511687.1:c.2261G= XP_011509989.1:p.Arg754=
XM_011511688.1:c.1586+3038G= XP_011509990.1:n.1586+3038G=
NM_001204.7:c.2261G= MANE Select NP_001195.2:p.Arg754=