Canonical Allele Identifier: CA1321556967
Gene: BMPR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202553155A= , CM000664.2:g.202553155A= GRCh38
NC_000002.11:g.203417878A= , CM000664.1:g.203417878A= GRCh37
NC_000002.10:g.203126123A= NCBI36
NG_009363.1:g.181829A= , LRG_712:g.181829A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1586+267A= MANE Select ENSP00000363708.4:n.1586+267A=
ENST00000638587.1:c.1517+267A= ENSP00000491062.1:n.1517+267A=
ENST00000374574.2:c.1586+267A= ENSP00000363702.2:n.1586+267A=
ENST00000374580.8:c.1586+267A= ENSP00000363708.4:n.1586+267A=
NM_001204.6:c.1586+267A= , LRG_712t1:c.1586+267A= NP_001195.2:n.1586+267A=
XM_011511687.1:c.1586+267A= XP_011509989.1:n.1586+267A=
XM_011511688.1:c.1586+267A= XP_011509990.1:n.1586+267A=
NM_001204.7:c.1586+267A= MANE Select NP_001195.2:n.1586+267A=
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