Canonical Allele Identifier: CA350340338

Gene: BMPR2

Linked Data

• ClinVar Variation Id: 618545
• ClinVar RCV Id: RCV000757032
• dbSNP Id: rs1559062859
• MyVariant Identifiers: chr2:g.203383635C>T (hg19) ; chr2:g.202518912C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202518912C>T , CM000664.2:g.202518912C>T	GRCh38
NC_000002.11:g.203383635C>T , CM000664.1:g.203383635C>T	GRCh37
NC_000002.10:g.203091880C>T	NCBI36
NG_009363.1:g.147586C>T , LRG_712:g.147586C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.712C>T MANE Select	ENSP00000363708.4:p.Gln238Ter
ENST00000638587.1:c.643C>T	ENSP00000491062.1:p.Gln215Ter
ENST00000374574.2:c.712C>T	ENSP00000363702.2:p.Gln238Ter
ENST00000374580.8:c.712C>T	ENSP00000363708.4:p.Gln238Ter
NM_001204.6:c.712C>T , LRG_712t1:c.712C>T	NP_001195.2:p.Gln238Ter
XM_011511687.1:c.712C>T	XP_011509989.1:p.Gln238Ter
XM_011511688.1:c.712C>T	XP_011509990.1:p.Gln238Ter
NM_001204.7:c.712C>T MANE Select	NP_001195.2:p.Gln238Ter