Canonical Allele Identifier: CA1321558887
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202555527C= , CM000664.2:g.202555527C= GRCh38
NC_000002.11:g.203420250C= , CM000664.1:g.203420250C= GRCh37
NC_000002.10:g.203128495C= NCBI36
NG_009363.1:g.184201C= , LRG_712:g.184201C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1862C= MANE Select ENSP00000363708.4:p.Thr621=
ENST00000638587.1:c.1793C= ENSP00000491062.1:n.1793C=
ENST00000374574.2:c.1586+2639C= ENSP00000363702.2:n.1586+2639C=
ENST00000374580.8:c.1862C= ENSP00000363708.4:p.Thr621=
NM_001204.6:c.1862C= , LRG_712t1:c.1862C= NP_001195.2:p.Thr621=
XM_011511687.1:c.1862C= XP_011509989.1:p.Thr621=
XM_011511688.1:c.1586+2639C= XP_011509990.1:n.1586+2639C=
NM_001204.7:c.1862C= MANE Select NP_001195.2:p.Thr621=