Canonical Allele Identifier: CA324334

Gene: BMPR2

Linked Data

• ClinVar Variation Id: 212812
• ClinVar RCV Id: RCV000199780
• dbSNP Id: rs863223421
• MyVariant Identifiers: chr2:g.203417484G>T (hg19) ; chr2:g.202552761G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202552761G>T , CM000664.2:g.202552761G>T	GRCh38
NC_000002.11:g.203417484G>T , CM000664.1:g.203417484G>T	GRCh37
NC_000002.10:g.203125729G>T	NCBI36
NG_009363.1:g.181435G>T , LRG_712:g.181435G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.1459G>T MANE Select	ENSP00000363708.4:p.Asp487Tyr
ENST00000638587.1:c.1390G>T	ENSP00000491062.1:p.Asp464Tyr
ENST00000374574.2:c.1459G>T	ENSP00000363702.2:p.Asp487Tyr
ENST00000374580.8:c.1459G>T	ENSP00000363708.4:p.Asp487Tyr
NM_001204.6:c.1459G>T , LRG_712t1:c.1459G>T	NP_001195.2:p.Asp487Tyr
XM_011511687.1:c.1459G>T	XP_011509989.1:p.Asp487Tyr
XM_011511688.1:c.1459G>T	XP_011509990.1:p.Asp487Tyr
NM_001204.7:c.1459G>T MANE Select	NP_001195.2:p.Asp487Tyr