Canonical Allele Identifier: CA1358522749

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38464411G= , CM000665.2:g.38464411G=	GRCh38
NC_000003.11:g.38505902G= , CM000665.1:g.38505902G=	GRCh37
NC_000003.10:g.38480906G=	NCBI36
NG_011791.1:g.15113G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000352511.5:c.52+10037G= MANE Select	ENSP00000340361.3:n.52+10037G=
ENST00000352511.4:c.52+10037G=	ENSP00000340361.3:n.52+10037G=
ENST00000465020.5:n.56+10037G=
NM_001106.3:c.52+10037G=	NP_001097.2:n.52+10037G=
XM_005265583.2:c.115+4722G=	XP_005265640.1:n.115+4722G=
XM_005265583.3:c.115+4722G=	XP_005265640.1:n.115+4722G=
XM_017007514.1:c.94+4743G=	XP_016863003.1:n.94+4743G=
XM_017007515.2:c.70+9727G=	XP_016863004.1:n.70+9727G=
NM_001106.4:c.52+10037G= MANE Select	NP_001097.2:n.52+10037G=