Canonical Allele Identifier: CA433138918

Gene: ACVR2B

Linked Data

• MyVariant Identifiers: chr3:g.38523964C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38482473C>G , CM000665.2:g.38482473C>G	GRCh38
NC_000003.11:g.38523964C>G , CM000665.1:g.38523964C>G	GRCh37
NC_000003.10:g.38498968C>G	NCBI36
NG_011791.1:g.33175C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352511.5:c.1257C>G MANE Select	ENSP00000340361.3:p.Gly419=
ENST00000352511.4:c.1257C>G	ENSP00000340361.3:p.Gly419=
ENST00000461232.1:n.5046C>G
ENST00000465020.5:n.1343C>G
NM_001106.3:c.1257C>G	NP_001097.2:p.Gly419=
XM_005265583.2:c.1320C>G	XP_005265640.1:p.Gly440=
XM_005265583.3:c.1320C>G	XP_005265640.1:p.Gly440=
XM_017007514.1:c.1299C>G	XP_016863003.1:p.Gly433=
XM_017007515.2:c.1275C>G	XP_016863004.1:p.Gly425=
XM_017007516.1:c.1254C>G	XP_016863005.1:p.Gly418=
NM_001106.4:c.1257C>G MANE Select	NP_001097.2:p.Gly419=