Canonical Allele Identifier: CA1321474695
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202377523A= , CM000664.2:g.202377523A= GRCh38
NC_000002.11:g.203242246A= , CM000664.1:g.203242246A= GRCh37
NC_000002.10:g.202950491A= NCBI36
NG_009363.1:g.6197A= , LRG_712:g.6197A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.49A= MANE Select ENSP00000363708.4:p.Thr17=
ENST00000374574.2:c.49A= ENSP00000363702.2:p.Thr17=
ENST00000374580.8:c.49A= ENSP00000363708.4:p.Thr17=
NM_001204.6:c.49A= , LRG_712t1:c.49A= NP_001195.2:p.Thr17=
XM_011511687.1:c.49A= XP_011509989.1:p.Thr17=
XM_011511688.1:c.49A= XP_011509990.1:p.Thr17=
NM_001204.7:c.49A= MANE Select NP_001195.2:p.Thr17=