Canonical Allele Identifier: CA386800616

Gene: OAS2

Linked Data

• dbSNP Id: rs15895
• MyVariant Identifiers: chr12:g.113448288A>C (hg19) ; chr12:g.113010483A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.113010483A>C , CM000674.2:g.113010483A>C	GRCh38
NC_000012.11:g.113448288A>C , CM000674.1:g.113448288A>C	GRCh37
NC_000012.10:g.111932671A>C	NCBI36
NG_029692.1:g.37015A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000392583.7:c.*1228A>C MANE Select	ENSP00000376362.3:n.*1228A>C
ENST00000679877.1:c.*3981A>C	ENSP00000506110.1:n.*3981A>C
ENST00000680122.1:c.*2503A>C	ENSP00000505194.1:n.*2503A>C
ENST00000680138.1:c.*2120A>C	ENSP00000506262.1:n.*2120A>C
ENST00000680898.1:n.3825A>C
ENST00000681023.1:n.3742A>C
ENST00000342315.8:c.2159A>C	ENSP00000342278.4:p.Ter720Ser
ENST00000392583.6:c.*1228A>C	ENSP00000376362.2:n.*1228A>C
ENST00000620097.1:c.2158-2A>C	ENSP00000483679.1:n.2158-2A>C
NM_002535.2:c.*1228A>C	NP_002526.2:n.*1228A>C
NM_016817.2:c.2159A>C	NP_058197.2:p.Ter720Ser
XM_011538415.1:c.2069A>C	XP_011536717.1:p.Ter690Ser
XR_001748725.2:n.3894A>C
NM_002535.3:c.*1228A>C MANE Select	NP_002526.2:n.*1228A>C
NM_016817.3:c.2159A>C	NP_058197.2:p.Ter720Ser