Canonical Allele Identifier: CA1477970132

Gene: BMPR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95154549G= , CM000666.2:g.95154549G=	GRCh38
NC_000004.11:g.96075700G= , CM000666.1:g.96075700G=	GRCh37
NC_000004.10:g.96294723G=	NCBI36
NG_009245.1:g.401573G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440890.7:c.1475G=	ENSP00000401907.2:p.Cys492=
ENST00000509540.6:c.1385G=	ENSP00000421671.1:p.Cys462=
ENST00000515059.6:c.1385G= MANE Select	ENSP00000426617.1:p.Cys462=
ENST00000672698.1:c.1385G=	ENSP00000500035.1:p.Cys462=
ENST00000264568.8:c.1385G=	ENSP00000264568.4:p.Cys462=
ENST00000394931.1:c.1385G=	ENSP00000378389.1:p.Cys462=
ENST00000440890.6:c.1475G=	ENSP00000401907.2:p.Cys492=
ENST00000509540.5:c.1385G=	ENSP00000421671.1:p.Cys462=
ENST00000512312.5:c.1385G=	ENSP00000425444.1:p.Cys462=
ENST00000515059.5:c.1385G=	ENSP00000426617.1:p.Cys462=
NM_001203.2:c.1385G=	NP_001194.1:p.Cys462=
NM_001256792.1:c.1385G=	NP_001243721.1:p.Cys462=
NM_001256793.1:c.1475G=	NP_001243722.1:p.Cys492=
NM_001256794.1:c.1385G=	NP_001243723.1:p.Cys462=
XM_011532201.1:c.1385G=	XP_011530503.1:p.Cys462=
XM_011532202.1:c.1385G=	XP_011530504.1:p.Cys462=
XM_011532201.2:c.1385G=	XP_011530503.1:p.Cys462=
XM_017008558.1:c.1385G=	XP_016864047.1:p.Cys462=
XM_017008559.1:c.1385G=	XP_016864048.1:p.Cys462=
XM_017008560.1:c.1385G=	XP_016864049.1:p.Cys462=
XM_017008561.1:c.1385G=	XP_016864050.1:p.Cys462=
NM_001203.3:c.1385G= MANE Select	NP_001194.1:p.Cys462=
NM_001256793.2:c.1475G=	NP_001243722.1:p.Cys492=
NM_001256792.2:c.1385G=	NP_001243721.1:p.Cys462=