Canonical Allele Identifier: CA1321556975
Gene: BMPR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202553184C= , CM000664.2:g.202553184C= GRCh38
NC_000002.11:g.203417907C= , CM000664.1:g.203417907C= GRCh37
NC_000002.10:g.203126152C= NCBI36
NG_009363.1:g.181858C= , LRG_712:g.181858C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1586+296C= MANE Select ENSP00000363708.4:n.1586+296C=
ENST00000638587.1:c.1517+296C= ENSP00000491062.1:n.1517+296C=
ENST00000374574.2:c.1586+296C= ENSP00000363702.2:n.1586+296C=
ENST00000374580.8:c.1586+296C= ENSP00000363708.4:n.1586+296C=
NM_001204.6:c.1586+296C= , LRG_712t1:c.1586+296C= NP_001195.2:n.1586+296C=
XM_011511687.1:c.1586+296C= XP_011509989.1:n.1586+296C=
XM_011511688.1:c.1586+296C= XP_011509990.1:n.1586+296C=
NM_001204.7:c.1586+296C= MANE Select NP_001195.2:n.1586+296C=
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