Canonical Allele Identifier: CA1321474478
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202377168A= , CM000664.2:g.202377168A= GRCh38
NC_000002.11:g.203241891A= , CM000664.1:g.203241891A= GRCh37
NC_000002.10:g.202950136A= NCBI36
NG_009363.1:g.5842A= , LRG_712:g.5842A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689938.1:c.57A= ENSP00000510443.1:p.Ter19=
ENST00000374580.10:c.-307A= MANE Select ENSP00000363708.4:n.-307A=
ENST00000374580.8:c.-307A= ENSP00000363708.4:n.-307A=
NM_001204.6:c.-307A= , LRG_712t1:c.-307A= NP_001195.2:n.-307A=
XM_011511687.1:c.-307A= XP_011509989.1:n.-307A=
XM_011511688.1:c.-307A= XP_011509990.1:n.-307A=
NM_001204.7:c.-307A= MANE Select NP_001195.2:n.-307A=