Canonical Allele Identifier: CA350341979
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 425907
dbSNP Id: rs1085307325

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202532715G>A , CM000664.2:g.202532715G>A GRCh38
NC_000002.11:g.203397438G>A , CM000664.1:g.203397438G>A GRCh37
NC_000002.10:g.203105683G>A NCBI36
NG_009363.1:g.161389G>A , LRG_712:g.161389G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.1259G>A MANE Select ENSP00000363708.4:p.Cys420Tyr
ENST00000638587.1:c.1190G>A ENSP00000491062.1:p.Cys397Tyr
ENST00000374574.2:c.1259G>A ENSP00000363702.2:p.Cys420Tyr
ENST00000374580.8:c.1259G>A ENSP00000363708.4:p.Cys420Tyr
NM_001204.6:c.1259G>A , LRG_712t1:c.1259G>A NP_001195.2:p.Cys420Tyr
XM_011511687.1:c.1259G>A XP_011509989.1:p.Cys420Tyr
XM_011511688.1:c.1259G>A XP_011509990.1:p.Cys420Tyr
NM_001204.7:c.1259G>A MANE Select NP_001195.2:p.Cys420Tyr