Canonical Allele Identifier: CA357326762

Gene: SCARB2

Linked Data

• COSMIC: COSM247192
• MyVariant Identifiers: chr4:g.77100726A>T (hg19) ; chr4:g.76179573A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179573A>T , CM000666.2:g.76179573A>T	GRCh38
NC_000004.11:g.77100726A>T , CM000666.1:g.77100726A>T	GRCh37
NC_000004.10:g.77319750A>T	NCBI36
NG_012054.1:g.39310T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.532T>A
ENST00000264896.8:c.556T>A MANE Select	ENSP00000264896.2:p.Ser186Thr
ENST00000502908.2:n.2057T>A
ENST00000638295.1:c.82T>A	ENSP00000492288.1:p.Ser28Thr
ENST00000638372.1:n.808T>A
ENST00000638603.1:c.556T>A	ENSP00000491728.1:p.Ser186Thr
ENST00000638663.1:c.556T>A	ENSP00000491407.1:p.Ser186Thr
ENST00000638680.1:n.2137T>A
ENST00000639145.1:c.547T>A	ENSP00000492831.1:p.Ser183Thr
ENST00000639300.1:c.556T>A	ENSP00000492840.1:p.Ser186Thr
ENST00000639324.1:n.655T>A
ENST00000639715.1:c.511T>A
ENST00000639738.1:c.276-13272T>A	ENSP00000491792.1:n.276-13272T>A
ENST00000640076.1:n.137T>A
ENST00000640341.1:c.*196T>A	ENSP00000492714.1:n.*196T>A
ENST00000640634.1:c.677T>A
ENST00000640640.1:c.556T>A	ENSP00000492246.1:p.Ser186Thr
ENST00000640916.1:n.484T>A
ENST00000640957.1:c.556T>A	ENSP00000492004.1:p.Ser186Thr
ENST00000264896.6:c.556T>A	ENSP00000264896.2:p.Ser186Thr
ENST00000452464.6:c.276-3663T>A	ENSP00000399154.2:n.276-3663T>A
NM_001204255.1:c.276-3663T>A	NP_001191184.1:n.276-3663T>A
NM_005506.3:c.556T>A	NP_005497.1:p.Ser186Thr
NM_005506.4:c.556T>A MANE Select	NP_005497.1:p.Ser186Thr
NM_001204255.2:c.276-3663T>A	NP_001191184.1:n.276-3663T>A