Canonical Allele Identifier: CA350399872
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202467681C>G , CM000664.2:g.202467681C>G GRCh38
NC_000002.11:g.203332404C>G , CM000664.1:g.203332404C>G GRCh37
NC_000002.10:g.203040649C>G NCBI36
NG_009363.1:g.96355C>G , LRG_712:g.96355C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.410C>G MANE Select ENSP00000363708.4:p.Thr137Arg
ENST00000638587.1:c.341C>G ENSP00000491062.1:p.Thr114Arg
ENST00000374574.2:c.410C>G ENSP00000363702.2:p.Thr137Arg
ENST00000374580.8:c.410C>G ENSP00000363708.4:p.Thr137Arg
ENST00000479069.1:n.317C>G
NM_001204.6:c.410C>G , LRG_712t1:c.410C>G NP_001195.2:p.Thr137Arg
XM_011511687.1:c.410C>G XP_011509989.1:p.Thr137Arg
XM_011511688.1:c.410C>G XP_011509990.1:p.Thr137Arg
NM_001204.7:c.410C>G MANE Select NP_001195.2:p.Thr137Arg