Canonical Allele Identifier: CA1358522787

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38464485G= , CM000665.2:g.38464485G=	GRCh38
NC_000003.11:g.38505976G= , CM000665.1:g.38505976G=	GRCh37
NC_000003.10:g.38480980G=	NCBI36
NG_011791.1:g.15187G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.52+10111G= MANE Select	ENSP00000340361.3:n.52+10111G=
ENST00000352511.4:c.52+10111G=	ENSP00000340361.3:n.52+10111G=
ENST00000465020.5:n.56+10111G=
NM_001106.3:c.52+10111G=	NP_001097.2:n.52+10111G=
XM_005265583.2:c.115+4796G=	XP_005265640.1:n.115+4796G=
XM_005265583.3:c.115+4796G=	XP_005265640.1:n.115+4796G=
XM_017007514.1:c.94+4817G=	XP_016863003.1:n.94+4817G=
XM_017007515.2:c.70+9801G=	XP_016863004.1:n.70+9801G=
NM_001106.4:c.52+10111G= MANE Select	NP_001097.2:n.52+10111G=