Canonical Allele Identifier: CA1358522751

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38464412T= , CM000665.2:g.38464412T=	GRCh38
NC_000003.11:g.38505903T= , CM000665.1:g.38505903T=	GRCh37
NC_000003.10:g.38480907T=	NCBI36
NG_011791.1:g.15114T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000352511.5:c.52+10038T= MANE Select	ENSP00000340361.3:n.52+10038T=
ENST00000352511.4:c.52+10038T=	ENSP00000340361.3:n.52+10038T=
ENST00000465020.5:n.56+10038T=
NM_001106.3:c.52+10038T=	NP_001097.2:n.52+10038T=
XM_005265583.2:c.115+4723T=	XP_005265640.1:n.115+4723T=
XM_005265583.3:c.115+4723T=	XP_005265640.1:n.115+4723T=
XM_017007514.1:c.94+4744T=	XP_016863003.1:n.94+4744T=
XM_017007515.2:c.70+9728T=	XP_016863004.1:n.70+9728T=
NM_001106.4:c.52+10038T= MANE Select	NP_001097.2:n.52+10038T=