Canonical Allele Identifier: CA350341821
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1359200084

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202532649A>C , CM000664.2:g.202532649A>C GRCh38
NC_000002.11:g.203397372A>C , CM000664.1:g.203397372A>C GRCh37
NC_000002.10:g.203105617A>C NCBI36
NG_009363.1:g.161323A>C , LRG_712:g.161323A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1193A>C MANE Select ENSP00000363708.4:p.Glu398Ala
ENST00000638587.1:c.1124A>C ENSP00000491062.1:p.Glu375Ala
ENST00000374574.2:c.1193A>C ENSP00000363702.2:p.Glu398Ala
ENST00000374580.8:c.1193A>C ENSP00000363708.4:p.Glu398Ala
NM_001204.6:c.1193A>C , LRG_712t1:c.1193A>C NP_001195.2:p.Glu398Ala
XM_011511687.1:c.1193A>C XP_011509989.1:p.Glu398Ala
XM_011511688.1:c.1193A>C XP_011509990.1:p.Glu398Ala
NM_001204.7:c.1193A>C MANE Select NP_001195.2:p.Glu398Ala