Canonical Allele Identifier: CA1358531509

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482499A= , CM000665.2:g.38482499A=	GRCh38
NC_000003.11:g.38523990A= , CM000665.1:g.38523990A=	GRCh37
NC_000003.10:g.38498994A=	NCBI36
NG_011791.1:g.33201A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1283A= MANE Select	ENSP00000340361.3:p.Gln428=
ENST00000352511.4:c.1283A=	ENSP00000340361.3:p.Gln428=
ENST00000461232.1:n.5072A=
ENST00000465020.5:n.1369A=
NM_001106.3:c.1283A=	NP_001097.2:p.Gln428=
XM_005265583.2:c.1346A=	XP_005265640.1:p.Gln449=
XM_005265583.3:c.1346A=	XP_005265640.1:p.Gln449=
XM_017007514.1:c.1325A=	XP_016863003.1:p.Gln442=
XM_017007515.2:c.1301A=	XP_016863004.1:p.Gln434=
XM_017007516.1:c.1280A=	XP_016863005.1:p.Gln427=
NM_001106.4:c.1283A= MANE Select	NP_001097.2:p.Gln428=