Canonical Allele Identifier: CA1358531494

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482479C= , CM000665.2:g.38482479C=	GRCh38
NC_000003.11:g.38523970C= , CM000665.1:g.38523970C=	GRCh37
NC_000003.10:g.38498974C=	NCBI36
NG_011791.1:g.33181C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1263C= MANE Select	ENSP00000340361.3:p.His421=
ENST00000352511.4:c.1263C=	ENSP00000340361.3:p.His421=
ENST00000461232.1:n.5052C=
ENST00000465020.5:n.1349C=
NM_001106.3:c.1263C=	NP_001097.2:p.His421=
XM_005265583.2:c.1326C=	XP_005265640.1:p.His442=
XM_005265583.3:c.1326C=	XP_005265640.1:p.His442=
XM_017007514.1:c.1305C=	XP_016863003.1:p.His435=
XM_017007515.2:c.1281C=	XP_016863004.1:p.His427=
XM_017007516.1:c.1260C=	XP_016863005.1:p.His420=
NM_001106.4:c.1263C= MANE Select	NP_001097.2:p.His421=