Canonical Allele Identifier: CA906884724
Gene: ACVR2B HGNC NCBI

Linked Data

dbSNP Id: rs1270932438
MyVariant Identifiers: chr3:g.38505926A>G (hg19) chr3:g.38464435A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38464435A>G , CM000665.2:g.38464435A>G GRCh38
NC_000003.11:g.38505926A>G , CM000665.1:g.38505926A>G GRCh37
NC_000003.10:g.38480930A>G NCBI36
NG_011791.1:g.15137A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000352511.5:c.52+10061A>G MANE Select ENSP00000340361.3:n.52+10061A>G
ENST00000352511.4:c.52+10061A>G ENSP00000340361.3:n.52+10061A>G
ENST00000465020.5:n.56+10061A>G
NM_001106.3:c.52+10061A>G NP_001097.2:n.52+10061A>G
XM_005265583.2:c.115+4746A>G XP_005265640.1:n.115+4746A>G
XM_005265583.3:c.115+4746A>G XP_005265640.1:n.115+4746A>G
XM_017007514.1:c.94+4767A>G XP_016863003.1:n.94+4767A>G
XM_017007515.2:c.70+9751A>G XP_016863004.1:n.70+9751A>G
NM_001106.4:c.52+10061A>G MANE Select NP_001097.2:n.52+10061A>G
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