Canonical Allele Identifier: CA1358530711

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38481354C= , CM000665.2:g.38481354C=	GRCh38
NC_000003.11:g.38522845C= , CM000665.1:g.38522845C=	GRCh37
NC_000003.10:g.38497849C=	NCBI36
NG_011791.1:g.32056C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.963C= MANE Select	ENSP00000340361.3:p.Asp321=
ENST00000352511.4:c.963C=	ENSP00000340361.3:p.Asp321=
ENST00000461232.1:n.4752C=
ENST00000465020.5:n.1049C=
NM_001106.3:c.963C=	NP_001097.2:p.Asp321=
XM_005265583.2:c.1026C=	XP_005265640.1:p.Asp342=
XM_005265583.3:c.1026C=	XP_005265640.1:p.Asp342=
XM_017007514.1:c.1005C=	XP_016863003.1:p.Asp335=
XM_017007515.2:c.981C=	XP_016863004.1:p.Asp327=
XM_017007516.1:c.960C=	XP_016863005.1:p.Asp320=
NM_001106.4:c.963C= MANE Select	NP_001097.2:p.Asp321=