Canonical Allele Identifier: CA1321539634
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202518803T= , CM000664.2:g.202518803T= GRCh38
NC_000002.11:g.203383526T= , CM000664.1:g.203383526T= GRCh37
NC_000002.10:g.203091771T= NCBI36
NG_009363.1:g.147477T= , LRG_712:g.147477T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.622-19T= MANE Select ENSP00000363708.4:n.622-19T=
ENST00000638587.1:c.553-19T= ENSP00000491062.1:n.553-19T=
ENST00000374574.2:c.622-19T= ENSP00000363702.2:n.622-19T=
ENST00000374580.8:c.622-19T= ENSP00000363708.4:n.622-19T=
NM_001204.6:c.622-19T= , LRG_712t1:c.622-19T= NP_001195.2:n.622-19T=
XM_011511687.1:c.622-19T= XP_011509989.1:n.622-19T=
XM_011511688.1:c.622-19T= XP_011509990.1:n.622-19T=
NM_001204.7:c.622-19T= MANE Select NP_001195.2:n.622-19T=