Canonical Allele Identifier: CA1469473840

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179391C= , CM000666.2:g.76179391C=	GRCh38
NC_000004.11:g.77100544C= , CM000666.1:g.77100544C=	GRCh37
NC_000004.10:g.77319568C=	NCBI36
NG_012054.1:g.39492G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.588+126G=
ENST00000264896.8:c.612+126G= MANE Select	ENSP00000264896.2:n.612+126G=
ENST00000502908.2:n.2239G=
ENST00000638295.1:c.138+126G=	ENSP00000492288.1:n.138+126G=
ENST00000638372.1:n.864+126G=
ENST00000638603.1:c.612+126G=	ENSP00000491728.1:n.612+126G=
ENST00000638663.1:c.612+126G=	ENSP00000491407.1:n.612+126G=
ENST00000638680.1:n.2193+126G=
ENST00000639145.1:c.603+126G=	ENSP00000492831.1:n.603+126G=
ENST00000639300.1:c.612+126G=	ENSP00000492840.1:n.612+126G=
ENST00000639324.1:n.711+126G=
ENST00000639715.1:c.567+126G=
ENST00000639738.1:c.276-13090G=	ENSP00000491792.1:n.276-13090G=
ENST00000640076.1:n.193+126G=
ENST00000640341.1:c.*252+126G=	ENSP00000492714.1:n.*252+126G=
ENST00000640634.1:c.733+126G=
ENST00000640640.1:c.612+126G=	ENSP00000492246.1:n.612+126G=
ENST00000640916.1:n.666G=
ENST00000640957.1:c.612+126G=	ENSP00000492004.1:n.612+126G=
ENST00000264896.6:c.612+126G=	ENSP00000264896.2:n.612+126G=
ENST00000452464.6:c.276-3481G=	ENSP00000399154.2:n.276-3481G=
NM_001204255.1:c.276-3481G=	NP_001191184.1:n.276-3481G=
NM_005506.3:c.612+126G=	NP_005497.1:n.612+126G=
NM_005506.4:c.612+126G= MANE Select	NP_005497.1:n.612+126G=
NM_001204255.2:c.276-3481G=	NP_001191184.1:n.276-3481G=