Canonical Allele Identifier: CA1321559647
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556098T= , CM000664.2:g.202556098T= GRCh38
NC_000002.11:g.203420821T= , CM000664.1:g.203420821T= GRCh37
NC_000002.10:g.203129066T= NCBI36
NG_009363.1:g.184772T= , LRG_712:g.184772T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2433T= MANE Select ENSP00000363708.4:p.Gly811=
ENST00000638587.1:c.2364T= ENSP00000491062.1:n.2364T=
ENST00000374574.2:c.1586+3210T= ENSP00000363702.2:n.1586+3210T=
ENST00000374580.8:c.2433T= ENSP00000363708.4:p.Gly811=
NM_001204.6:c.2433T= , LRG_712t1:c.2433T= NP_001195.2:p.Gly811=
XM_011511687.1:c.2433T= XP_011509989.1:p.Gly811=
XM_011511688.1:c.1586+3210T= XP_011509990.1:n.1586+3210T=
NM_001204.7:c.2433T= MANE Select NP_001195.2:p.Gly811=