Canonical Allele Identifier: CA64533038
Gene: BMPR2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12468226

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202472278A>G , CM000664.2:g.202472278A>G GRCh38
NC_000002.10:g.203045246A>G NCBI36
NC_000002.11:g.203337001A>G , CM000664.1:g.203337001A>G GRCh37
NG_009363.1:g.100952A>G , LRG_712:g.100952A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374574.2:c.418+4589A>G ENSP00000363702.2:p.=
ENST00000374580.8:c.418+4589A>G ENSP00000363708.4:p.=
ENST00000479069.1:n.326-2430A>G
NM_001204.6:c.418+4589A>G , LRG_712t1:c.418+4589A>G NP_001195.2:p.=
XM_011511687.1:c.418+4589A>G XP_011509989.1:p.=
XM_011511688.1:c.418+4589A>G XP_011509990.1:p.=