Canonical Allele Identifier: CA1358531331

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482356T= , CM000665.2:g.38482356T=	GRCh38
NC_000003.11:g.38523847T= , CM000665.1:g.38523847T=	GRCh37
NC_000003.10:g.38498851T=	NCBI36
NG_011791.1:g.33058T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1213+20T= MANE Select	ENSP00000340361.3:n.1213+20T=
ENST00000352511.4:c.1213+20T=	ENSP00000340361.3:n.1213+20T=
ENST00000461232.1:n.5002+20T=
ENST00000465020.5:n.1299+20T=
NM_001106.3:c.1213+20T=	NP_001097.2:n.1213+20T=
XM_005265583.2:c.1276+20T=	XP_005265640.1:n.1276+20T=
XM_005265583.3:c.1276+20T=	XP_005265640.1:n.1276+20T=
XM_017007514.1:c.1255+20T=	XP_016863003.1:n.1255+20T=
XM_017007515.2:c.1231+20T=	XP_016863004.1:n.1231+20T=
XM_017007516.1:c.1210+20T=	XP_016863005.1:n.1210+20T=
NM_001106.4:c.1213+20T= MANE Select	NP_001097.2:n.1213+20T=