Canonical Allele Identifier: CA350344421
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202552725T>A , CM000664.2:g.202552725T>A GRCh38
NC_000002.11:g.203417448T>A , CM000664.1:g.203417448T>A GRCh37
NC_000002.10:g.203125693T>A NCBI36
NG_009363.1:g.181399T>A , LRG_712:g.181399T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1423T>A MANE Select ENSP00000363708.4:p.Ser475Thr
ENST00000638587.1:c.1354T>A ENSP00000491062.1:p.Ser452Thr
ENST00000374574.2:c.1423T>A ENSP00000363702.2:p.Ser475Thr
ENST00000374580.8:c.1423T>A ENSP00000363708.4:p.Ser475Thr
NM_001204.6:c.1423T>A , LRG_712t1:c.1423T>A NP_001195.2:p.Ser475Thr
XM_011511687.1:c.1423T>A XP_011509989.1:p.Ser475Thr
XM_011511688.1:c.1423T>A XP_011509990.1:p.Ser475Thr
NM_001204.7:c.1423T>A MANE Select NP_001195.2:p.Ser475Thr