Canonical Allele Identifier: CA15770891

Gene: OAS2

Linked Data

• dbSNP Id: rs1293773
• gnomAD v2: 12-113420551-T-C
• gnomAD v3: 12-112982746-T-C
• gnomAD v4: 12-112982746-T-C
• MyVariant Identifiers: chr12:g.113420551T>C (hg19) ; chr12:g.112982746T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112982746T>C , CM000674.2:g.112982746T>C	GRCh38
NC_000012.11:g.113420551T>C , CM000674.1:g.113420551T>C	GRCh37
NC_000012.10:g.111904934T>C	NCBI36
NG_029692.1:g.9278T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392583.7:c.177+3961T>C MANE Select	ENSP00000376362.3:n.177+3961T>C
ENST00000551603.2:c.177+3961T>C	ENSP00000450307.2:n.177+3961T>C
ENST00000552756.6:c.177+3961T>C	ENSP00000446977.2:n.177+3961T>C
ENST00000620097.2:c.69+3961T>C	ENSP00000483679.2:n.69+3961T>C
ENST00000679877.1:c.177+3961T>C	ENSP00000506110.1:n.177+3961T>C
ENST00000680122.1:c.177+3961T>C	ENSP00000505194.1:n.177+3961T>C
ENST00000680138.1:c.177+3961T>C	ENSP00000506262.1:n.177+3961T>C
ENST00000680514.1:c.177+3961T>C	ENSP00000505771.1:n.177+3961T>C
ENST00000680666.1:n.1196+2957T>C
ENST00000680685.1:c.248+2957T>C	ENSP00000505554.1:n.248+2957T>C
ENST00000680898.1:n.200+3961T>C
ENST00000681673.1:n.267+3961T>C
ENST00000342315.8:c.177+3961T>C	ENSP00000342278.4:n.177+3961T>C
ENST00000392583.6:c.177+3961T>C	ENSP00000376362.2:n.177+3961T>C
ENST00000449768.2:c.177+3961T>C	ENSP00000411763.2:n.177+3961T>C
ENST00000551603.1:c.177+3961T>C	ENSP00000450307.1:n.177+3961T>C
ENST00000552756.5:c.177+3961T>C	ENSP00000446977.1:n.177+3961T>C
ENST00000620097.1:c.177+3961T>C	ENSP00000483679.1:n.177+3961T>C
NM_001032731.1:c.177+3961T>C	NP_001027903.1:n.177+3961T>C
NM_002535.2:c.177+3961T>C	NP_002526.2:n.177+3961T>C
NM_016817.2:c.177+3961T>C	NP_058197.2:n.177+3961T>C
XM_011538415.1:c.87+2957T>C	XP_011536717.1:n.87+2957T>C
XR_001748725.2:n.320+3961T>C
NM_001032731.2:c.177+3961T>C	NP_001027903.1:n.177+3961T>C
NM_002535.3:c.177+3961T>C MANE Select	NP_002526.2:n.177+3961T>C
NM_016817.3:c.177+3961T>C	NP_058197.2:n.177+3961T>C