Canonical Allele Identifier: CA10576586
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 228460
dbSNP Id: rs876657748

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202520135T>C , CM000664.2:g.202520135T>C GRCh38
NC_000002.11:g.203384858T>C , CM000664.1:g.203384858T>C GRCh37
NC_000002.10:g.203093103T>C NCBI36
NG_009363.1:g.148809T>C , LRG_712:g.148809T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.901T>C MANE Select ENSP00000363708.4:p.Ser301Pro
ENST00000638587.1:c.832T>C ENSP00000491062.1:p.Ser278Pro
ENST00000374574.2:c.901T>C ENSP00000363702.2:p.Ser301Pro
ENST00000374580.8:c.901T>C ENSP00000363708.4:p.Ser301Pro
NM_001204.6:c.901T>C , LRG_712t1:c.901T>C NP_001195.2:p.Ser301Pro
XM_011511687.1:c.901T>C XP_011509989.1:p.Ser301Pro
XM_011511688.1:c.901T>C XP_011509990.1:p.Ser301Pro
NM_001204.7:c.901T>C MANE Select NP_001195.2:p.Ser301Pro