Canonical Allele Identifier: CA2061535
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1157504
ClinVar RCV Id: RCV001500604
dbSNP Id: rs201938348

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556118C>T , CM000664.2:g.202556118C>T GRCh38
NC_000002.11:g.203420841C>T , CM000664.1:g.203420841C>T GRCh37
NC_000002.10:g.203129086C>T NCBI36
NG_009363.1:g.184792C>T , LRG_712:g.184792C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2453C>T MANE Select ENSP00000363708.4:p.Ser818Phe
ENST00000638587.1:c.2384C>T ENSP00000491062.1:n.2384C>T
ENST00000374574.2:c.1586+3230C>T ENSP00000363702.2:n.1586+3230C>T
ENST00000374580.8:c.2453C>T ENSP00000363708.4:p.Ser818Phe
NM_001204.6:c.2453C>T , LRG_712t1:c.2453C>T NP_001195.2:p.Ser818Phe
XM_011511687.1:c.2453C>T XP_011509989.1:p.Ser818Phe
XM_011511688.1:c.1586+3230C>T XP_011509990.1:n.1586+3230C>T
NM_001204.7:c.2453C>T MANE Select NP_001195.2:p.Ser818Phe