Canonical Allele Identifier: CA72926329

Gene: ACVR2B

Linked Data

• dbSNP Id: rs530383572
• MyVariant Identifiers: chr3:g.38523872G>A (hg19) ; chr3:g.38482381G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482381G>A , CM000665.2:g.38482381G>A	GRCh38
NC_000003.11:g.38523872G>A , CM000665.1:g.38523872G>A	GRCh37
NC_000003.10:g.38498876G>A	NCBI36
NG_011791.1:g.33083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1213+45G>A MANE Select	ENSP00000340361.3:n.1213+45G>A
ENST00000352511.4:c.1213+45G>A	ENSP00000340361.3:n.1213+45G>A
ENST00000461232.1:n.5002+45G>A
ENST00000465020.5:n.1299+45G>A
NM_001106.3:c.1213+45G>A	NP_001097.2:n.1213+45G>A
XM_005265583.2:c.1276+45G>A	XP_005265640.1:n.1276+45G>A
XM_005265583.3:c.1276+45G>A	XP_005265640.1:n.1276+45G>A
XM_017007514.1:c.1255+45G>A	XP_016863003.1:n.1255+45G>A
XM_017007515.2:c.1231+45G>A	XP_016863004.1:n.1231+45G>A
XM_017007516.1:c.1210+45G>A	XP_016863005.1:n.1210+45G>A
NM_001106.4:c.1213+45G>A MANE Select	NP_001097.2:n.1213+45G>A