Canonical Allele Identifier: CA2665095693

Gene: ACVR2B

Linked Data

• gnomAD v4: 3-38482365-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482366del , CM000665.2:g.38482366del	GRCh38
NC_000003.11:g.38523857del , CM000665.1:g.38523857del	GRCh37
NC_000003.10:g.38498861del	NCBI36
NG_011791.1:g.33068del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1213+30del MANE Select	ENSP00000340361.3:n.1213+30del
ENST00000352511.4:c.1213+30del	ENSP00000340361.3:n.1213+30del
ENST00000461232.1:n.5002+30del
ENST00000465020.5:n.1299+30del
NM_001106.3:c.1213+30del	NP_001097.2:n.1213+30del
XM_005265583.2:c.1276+30del	XP_005265640.1:n.1276+30del
XM_005265583.3:c.1276+30del	XP_005265640.1:n.1276+30del
XM_017007514.1:c.1255+30del	XP_016863003.1:n.1255+30del
XM_017007515.2:c.1231+30del	XP_016863004.1:n.1231+30del
XM_017007516.1:c.1210+30del	XP_016863005.1:n.1210+30del
NM_001106.4:c.1213+30del MANE Select	NP_001097.2:n.1213+30del