Canonical Allele Identifier: CA350399066
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202464838T>G , CM000664.2:g.202464838T>G GRCh38
NC_000002.11:g.203329561T>G , CM000664.1:g.203329561T>G GRCh37
NC_000002.10:g.203037806T>G NCBI36
NG_009363.1:g.93512T>G , LRG_712:g.93512T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.106T>G MANE Select ENSP00000363708.4:p.Phe36Val
ENST00000638587.1:c.31T>G ENSP00000491062.1:p.Phe11Val
ENST00000374574.2:c.106T>G ENSP00000363702.2:p.Phe36Val
ENST00000374580.8:c.106T>G ENSP00000363708.4:p.Phe36Val
ENST00000479069.1:n.13T>G
NM_001204.6:c.106T>G , LRG_712t1:c.106T>G NP_001195.2:p.Phe36Val
XM_011511687.1:c.106T>G XP_011509989.1:p.Phe36Val
XM_011511688.1:c.106T>G XP_011509990.1:p.Phe36Val
NM_001204.7:c.106T>G MANE Select NP_001195.2:p.Phe36Val