Canonical Allele Identifier: CA1321507978
Gene: BMPR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202464995C= , CM000664.2:g.202464995C= GRCh38
NC_000002.11:g.203329718C= , CM000664.1:g.203329718C= GRCh37
NC_000002.10:g.203037963C= NCBI36
NG_009363.1:g.93669C= , LRG_712:g.93669C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.247+16C= MANE Select ENSP00000363708.4:n.247+16C=
ENST00000638587.1:c.176+12C= ENSP00000491062.1:n.176+12C=
ENST00000374574.2:c.247+16C= ENSP00000363702.2:n.247+16C=
ENST00000374580.8:c.247+16C= ENSP00000363708.4:n.247+16C=
ENST00000479069.1:n.154+16C=
NM_001204.6:c.247+16C= , LRG_712t1:c.247+16C= NP_001195.2:n.247+16C=
XM_011511687.1:c.247+16C= XP_011509989.1:n.247+16C=
XM_011511688.1:c.247+16C= XP_011509990.1:n.247+16C=
NM_001204.7:c.247+16C= MANE Select NP_001195.2:n.247+16C=
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