Canonical Allele Identifier: CA430905549
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203420996T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556273T>C , CM000664.2:g.202556273T>C GRCh38
NC_000002.11:g.203420996T>C , CM000664.1:g.203420996T>C GRCh37
NC_000002.10:g.203129241T>C NCBI36
NG_009363.1:g.184947T>C , LRG_712:g.184947T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2608T>C MANE Select ENSP00000363708.4:p.Leu870=
ENST00000638587.1:c.2539T>C ENSP00000491062.1:n.2539T>C
ENST00000374574.2:c.1586+3385T>C ENSP00000363702.2:n.1586+3385T>C
ENST00000374580.8:c.2608T>C ENSP00000363708.4:p.Leu870=
NM_001204.6:c.2608T>C , LRG_712t1:c.2608T>C NP_001195.2:p.Leu870=
XM_011511687.1:c.2608T>C XP_011509989.1:p.Leu870=
XM_011511688.1:c.1586+3385T>C XP_011509990.1:n.1586+3385T>C
NM_001204.7:c.2608T>C MANE Select NP_001195.2:p.Leu870=