Canonical Allele Identifier: CA916873595

Gene: ACVR2B

Linked Data

• dbSNP Id: rs1559647574

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38464378_38464380dup , CM000665.2:g.38464378_38464380dup	GRCh38
NC_000003.11:g.38505869_38505871dup , CM000665.1:g.38505869_38505871dup	GRCh37
NC_000003.10:g.38480873_38480875dup	NCBI36
NG_011791.1:g.15080_15082dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000352511.5:c.52+10004_52+10006dup MANE Select	ENSP00000340361.3:n.52+10004_52+10006dup
ENST00000352511.4:c.52+10004_52+10006dup	ENSP00000340361.3:n.52+10004_52+10006dup
ENST00000465020.5:n.56+10004_56+10006dup
NM_001106.3:c.52+10004_52+10006dup	NP_001097.2:n.52+10004_52+10006dup
XM_005265583.2:c.115+4689_115+4691dup	XP_005265640.1:n.115+4689_115+4691dup
XM_005265583.3:c.115+4689_115+4691dup	XP_005265640.1:n.115+4689_115+4691dup
XM_017007514.1:c.94+4710_94+4712dup	XP_016863003.1:n.94+4710_94+4712dup
XM_017007515.2:c.70+9694_70+9696dup	XP_016863004.1:n.70+9694_70+9696dup
NM_001106.4:c.52+10004_52+10006dup MANE Select	NP_001097.2:n.52+10004_52+10006dup