Canonical Allele Identifier: CA1358530702

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38481337A= , CM000665.2:g.38481337A=	GRCh38
NC_000003.11:g.38522828A= , CM000665.1:g.38522828A=	GRCh37
NC_000003.10:g.38497832A=	NCBI36
NG_011791.1:g.32039A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000352511.5:c.960-14A= MANE Select	ENSP00000340361.3:n.960-14A=
ENST00000352511.4:c.960-14A=	ENSP00000340361.3:n.960-14A=
ENST00000461232.1:n.4749-14A=
ENST00000465020.5:n.1046-14A=
NM_001106.3:c.960-14A=	NP_001097.2:n.960-14A=
XM_005265583.2:c.1023-14A=	XP_005265640.1:n.1023-14A=
XM_005265583.3:c.1023-14A=	XP_005265640.1:n.1023-14A=
XM_017007514.1:c.1002-14A=	XP_016863003.1:n.1002-14A=
XM_017007515.2:c.978-14A=	XP_016863004.1:n.978-14A=
XM_017007516.1:c.957-14A=	XP_016863005.1:n.957-14A=
NM_001106.4:c.960-14A= MANE Select	NP_001097.2:n.960-14A=