Canonical Allele Identifier: CA2036281399

Gene: ACVR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51987279A= , CM000674.2:g.51987279A=	GRCh38
NC_000012.11:g.52381063A= , CM000674.1:g.52381063A=	GRCh37
NC_000012.10:g.50667330A=	NCBI36
NG_022926.1:g.40613A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257963.9:c.1261+337A= MANE Select	ENSP00000257963.4:n.1261+337A=
ENST00000257963.8:c.1261+337A=	ENSP00000257963.4:n.1261+337A=
ENST00000415850.6:c.1598A=	ENSP00000397550.2:n.1598A=
ENST00000426655.6:c.1261+337A=	ENSP00000390477.2:n.1261+337A=
ENST00000541224.5:c.1384+337A=	ENSP00000442656.1:n.1384+337A=
ENST00000542485.1:c.1105+337A=	ENSP00000442885.1:n.1105+337A=
ENST00000563121.1:n.289+1931A=
NM_004302.4:c.1261+337A=	NP_004293.1:n.1261+337A=
NM_020327.3:c.1105+337A=	NP_064732.3:n.1105+337A=
NM_020328.3:c.1384+337A=	NP_064733.3:n.1384+337A=
XM_011538966.1:c.1259+1931A=	XP_011537268.1:n.1259+1931A=
XM_011538966.3:c.1259+1931A=	XP_011537268.1:n.1259+1931A=
XM_017020201.2:c.1136+1931A=	XP_016875690.1:n.1136+1931A=
NM_004302.5:c.1261+337A= MANE Select	NP_004293.1:n.1261+337A=
NM_020328.4:c.1384+337A=	NP_064733.3:n.1384+337A=
NM_020327.4:c.1105+337A=	NP_064732.3:n.1105+337A=