Canonical Allele Identifier: CA430840407
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203384842A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202520119A>G , CM000664.2:g.202520119A>G GRCh38
NC_000002.11:g.203384842A>G , CM000664.1:g.203384842A>G GRCh37
NC_000002.10:g.203093087A>G NCBI36
NG_009363.1:g.148793A>G , LRG_712:g.148793A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.885A>G MANE Select ENSP00000363708.4:p.Thr295=
ENST00000638587.1:c.816A>G ENSP00000491062.1:p.Thr272=
ENST00000374574.2:c.885A>G ENSP00000363702.2:p.Thr295=
ENST00000374580.8:c.885A>G ENSP00000363708.4:p.Thr295=
NM_001204.6:c.885A>G , LRG_712t1:c.885A>G NP_001195.2:p.Thr295=
XM_011511687.1:c.885A>G XP_011509989.1:p.Thr295=
XM_011511688.1:c.885A>G XP_011509990.1:p.Thr295=
NM_001204.7:c.885A>G MANE Select NP_001195.2:p.Thr295=