Canonical Allele Identifier: CA1321560296
Gene: BMPR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556572G= , CM000664.2:g.202556572G= GRCh38
NC_000002.11:g.203421295G= , CM000664.1:g.203421295G= GRCh37
NC_000002.10:g.203129540G= NCBI36
NG_009363.1:g.185246G= , LRG_712:g.185246G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2866+41G= MANE Select ENSP00000363708.4:n.2866+41G=
ENST00000638587.1:c.2797+41G= ENSP00000491062.1:n.2797+41G=
ENST00000374574.2:c.1587-3124G= ENSP00000363702.2:n.1587-3124G=
ENST00000374580.8:c.2866+41G= ENSP00000363708.4:n.2866+41G=
NM_001204.6:c.2866+41G= , LRG_712t1:c.2866+41G= NP_001195.2:n.2866+41G=
XM_011511687.1:c.2866+41G= XP_011509989.1:n.2866+41G=
XM_011511688.1:c.1587-3124G= XP_011509990.1:n.1587-3124G=
NM_001204.7:c.2866+41G= MANE Select NP_001195.2:n.2866+41G=
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