Canonical Allele Identifier: CA1358528889

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38477263G= , CM000665.2:g.38477263G=	GRCh38
NC_000003.11:g.38518754G= , CM000665.1:g.38518754G=	GRCh37
NC_000003.10:g.38493758G=	NCBI36
NG_011791.1:g.27965G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000352511.5:c.53-24G= MANE Select	ENSP00000340361.3:n.53-24G=
ENST00000352511.4:c.53-24G=	ENSP00000340361.3:n.53-24G=
ENST00000461232.1:n.3818G=
ENST00000465020.5:n.57-24G=
NM_001106.3:c.53-24G=	NP_001097.2:n.53-24G=
XM_005265583.2:c.116-24G=	XP_005265640.1:n.116-24G=
XM_005265583.3:c.116-24G=	XP_005265640.1:n.116-24G=
XM_017007514.1:c.95-24G=	XP_016863003.1:n.95-24G=
XM_017007515.2:c.71-24G=	XP_016863004.1:n.71-24G=
XM_017007516.1:c.50-24G=	XP_016863005.1:n.50-24G=
NM_001106.4:c.53-24G= MANE Select	NP_001097.2:n.53-24G=