Canonical Allele Identifier: CA906884712
Gene: ACVR2B HGNC NCBI

Linked Data

dbSNP Id: rs564036685
MyVariant Identifiers: chr3:g.38505895T>A (hg19) chr3:g.38464404T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38464404T>A , CM000665.2:g.38464404T>A GRCh38
NC_000003.11:g.38505895T>A , CM000665.1:g.38505895T>A GRCh37
NC_000003.10:g.38480899T>A NCBI36
NG_011791.1:g.15106T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000352511.5:c.52+10030T>A MANE Select ENSP00000340361.3:n.52+10030T>A
ENST00000352511.4:c.52+10030T>A ENSP00000340361.3:n.52+10030T>A
ENST00000465020.5:n.56+10030T>A
NM_001106.3:c.52+10030T>A NP_001097.2:n.52+10030T>A
XM_005265583.2:c.115+4715T>A XP_005265640.1:n.115+4715T>A
XM_005265583.3:c.115+4715T>A XP_005265640.1:n.115+4715T>A
XM_017007514.1:c.94+4736T>A XP_016863003.1:n.94+4736T>A
XM_017007515.2:c.70+9720T>A XP_016863004.1:n.70+9720T>A
NM_001106.4:c.52+10030T>A MANE Select NP_001097.2:n.52+10030T>A
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