Canonical Allele Identifier: CA430838583
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203379666A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202514943A>G , CM000664.2:g.202514943A>G GRCh38
NC_000002.11:g.203379666A>G , CM000664.1:g.203379666A>G GRCh37
NC_000002.10:g.203087911A>G NCBI36
NG_009363.1:g.143617A>G , LRG_712:g.143617A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.585A>G MANE Select ENSP00000363708.4:p.Glu195=
ENST00000638587.1:c.516A>G ENSP00000491062.1:p.Glu172=
ENST00000374574.2:c.585A>G ENSP00000363702.2:p.Glu195=
ENST00000374580.8:c.585A>G ENSP00000363708.4:p.Glu195=
NM_001204.6:c.585A>G , LRG_712t1:c.585A>G NP_001195.2:p.Glu195=
XM_011511687.1:c.585A>G XP_011509989.1:p.Glu195=
XM_011511688.1:c.585A>G XP_011509990.1:p.Glu195=
NM_001204.7:c.585A>G MANE Select NP_001195.2:p.Glu195=