Canonical Allele Identifier: CA1358531420

Gene: ACVR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482416_38482417delinsTC , CM000665.2:g.38482416_38482417delinsTC	GRCh38
NC_000003.11:g.38523907_38523908delinsTC , CM000665.1:g.38523907_38523908delinsTC	GRCh37
NC_000003.10:g.38498911_38498912delinsTC	NCBI36
NG_011791.1:g.33118_33119delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1214-14_1214-13delinsTC MANE Select	ENSP00000340361.3:n.1214-14_1214-13delinsTC
ENST00000352511.4:c.1214-14_1214-13delinsTC	ENSP00000340361.3:n.1214-14_1214-13delinsTC
ENST00000461232.1:n.5003-14_5003-13delinsTC
ENST00000465020.5:n.1300-14_1300-13delinsTC
NM_001106.3:c.1214-14_1214-13delinsTC	NP_001097.2:n.1214-14_1214-13delinsTC
XM_005265583.2:c.1277-14_1277-13delinsTC	XP_005265640.1:n.1277-14_1277-13delinsTC
XM_005265583.3:c.1277-14_1277-13delinsTC	XP_005265640.1:n.1277-14_1277-13delinsTC
XM_017007514.1:c.1256-14_1256-13delinsTC	XP_016863003.1:n.1256-14_1256-13delinsTC
XM_017007515.2:c.1232-14_1232-13delinsTC	XP_016863004.1:n.1232-14_1232-13delinsTC
XM_017007516.1:c.1211-14_1211-13delinsTC	XP_016863005.1:n.1211-14_1211-13delinsTC
NM_001106.4:c.1214-14_1214-13delinsTC MANE Select	NP_001097.2:n.1214-14_1214-13delinsTC