Canonical Allele Identifier: CA352134812

Gene: ACVR2B

Linked Data

• MyVariant Identifiers: chr3:g.38523967G>C (hg19) ; chr3:g.38482476G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482476G>C , CM000665.2:g.38482476G>C	GRCh38
NC_000003.11:g.38523967G>C , CM000665.1:g.38523967G>C	GRCh37
NC_000003.10:g.38498971G>C	NCBI36
NG_011791.1:g.33178G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1260G>C MANE Select	ENSP00000340361.3:p.Gln420His
ENST00000352511.4:c.1260G>C	ENSP00000340361.3:p.Gln420His
ENST00000461232.1:n.5049G>C
ENST00000465020.5:n.1346G>C
NM_001106.3:c.1260G>C	NP_001097.2:p.Gln420His
XM_005265583.2:c.1323G>C	XP_005265640.1:p.Gln441His
XM_005265583.3:c.1323G>C	XP_005265640.1:p.Gln441His
XM_017007514.1:c.1302G>C	XP_016863003.1:p.Gln434His
XM_017007515.2:c.1278G>C	XP_016863004.1:p.Gln426His
XM_017007516.1:c.1257G>C	XP_016863005.1:p.Gln419His
NM_001106.4:c.1260G>C MANE Select	NP_001097.2:p.Gln420His