Canonical Allele Identifier: CA1358531279

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482320C= , CM000665.2:g.38482320C=	GRCh38
NC_000003.11:g.38523811C= , CM000665.1:g.38523811C=	GRCh37
NC_000003.10:g.38498815C=	NCBI36
NG_011791.1:g.33022C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1197C= MANE Select	ENSP00000340361.3:p.Arg399=
ENST00000352511.4:c.1197C=	ENSP00000340361.3:p.Arg399=
ENST00000461232.1:n.4986C=
ENST00000465020.5:n.1283C=
NM_001106.3:c.1197C=	NP_001097.2:p.Arg399=
XM_005265583.2:c.1260C=	XP_005265640.1:p.Arg420=
XM_005265583.3:c.1260C=	XP_005265640.1:p.Arg420=
XM_017007514.1:c.1239C=	XP_016863003.1:p.Arg413=
XM_017007515.2:c.1215C=	XP_016863004.1:p.Arg405=
XM_017007516.1:c.1194C=	XP_016863005.1:p.Arg398=
NM_001106.4:c.1197C= MANE Select	NP_001097.2:p.Arg399=