Canonical Allele Identifier: CA1358531525

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482504G= , CM000665.2:g.38482504G=	GRCh38
NC_000003.11:g.38523995G= , CM000665.1:g.38523995G=	GRCh37
NC_000003.10:g.38498999G=	NCBI36
NG_011791.1:g.33206G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1288G= MANE Select	ENSP00000340361.3:p.Val430=
ENST00000352511.4:c.1288G=	ENSP00000340361.3:p.Val430=
ENST00000461232.1:n.5077G=
ENST00000465020.5:n.1374G=
NM_001106.3:c.1288G=	NP_001097.2:p.Val430=
XM_005265583.2:c.1351G=	XP_005265640.1:p.Val451=
XM_005265583.3:c.1351G=	XP_005265640.1:p.Val451=
XM_017007514.1:c.1330G=	XP_016863003.1:p.Val444=
XM_017007515.2:c.1306G=	XP_016863004.1:p.Val436=
XM_017007516.1:c.1285G=	XP_016863005.1:p.Val429=
NM_001106.4:c.1288G= MANE Select	NP_001097.2:p.Val430=