Canonical Allele Identifier: CA1358530684

Gene: ACVR2B

Linked Data

• dbSNP Id: rs1710013674

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38481296A>T , CM000665.2:g.38481296A>T	GRCh38
NC_000003.11:g.38522787A>T , CM000665.1:g.38522787A>T	GRCh37
NC_000003.10:g.38497791A>T	NCBI36
NG_011791.1:g.31998A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.960-55A>T MANE Select	ENSP00000340361.3:n.960-55A>T
ENST00000352511.4:c.960-55A>T	ENSP00000340361.3:n.960-55A>T
ENST00000461232.1:n.4749-55A>T
ENST00000465020.5:n.1046-55A>T
NM_001106.3:c.960-55A>T	NP_001097.2:n.960-55A>T
XM_005265583.2:c.1023-55A>T	XP_005265640.1:n.1023-55A>T
XM_005265583.3:c.1023-55A>T	XP_005265640.1:n.1023-55A>T
XM_017007514.1:c.1002-55A>T	XP_016863003.1:n.1002-55A>T
XM_017007515.2:c.978-55A>T	XP_016863004.1:n.978-55A>T
XM_017007516.1:c.957-55A>T	XP_016863005.1:n.957-55A>T
NM_001106.4:c.960-55A>T MANE Select	NP_001097.2:n.960-55A>T