Canonical Allele Identifier: CA1358522757

Gene: ACVR2B

Linked Data

• dbSNP Id: rs1709697413

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38464425_38464426dup , CM000665.2:g.38464425_38464426dup	GRCh38
NC_000003.11:g.38505916_38505917dup , CM000665.1:g.38505916_38505917dup	GRCh37
NC_000003.10:g.38480920_38480921dup	NCBI36
NG_011791.1:g.15127_15128dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000352511.5:c.52+10051_52+10052dup MANE Select	ENSP00000340361.3:n.52+10051_52+10052dup
ENST00000352511.4:c.52+10051_52+10052dup	ENSP00000340361.3:n.52+10051_52+10052dup
ENST00000465020.5:n.56+10051_56+10052dup
NM_001106.3:c.52+10051_52+10052dup	NP_001097.2:n.52+10051_52+10052dup
XM_005265583.2:c.115+4736_115+4737dup	XP_005265640.1:n.115+4736_115+4737dup
XM_005265583.3:c.115+4736_115+4737dup	XP_005265640.1:n.115+4736_115+4737dup
XM_017007514.1:c.94+4757_94+4758dup	XP_016863003.1:n.94+4757_94+4758dup
XM_017007515.2:c.70+9741_70+9742dup	XP_016863004.1:n.70+9741_70+9742dup
NM_001106.4:c.52+10051_52+10052dup MANE Select	NP_001097.2:n.52+10051_52+10052dup