Canonical Allele Identifier: CA1469473735

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179331G= , CM000666.2:g.76179331G=	GRCh38
NC_000004.11:g.77100484G= , CM000666.1:g.77100484G=	GRCh37
NC_000004.10:g.77319508G=	NCBI36
NG_012054.1:g.39552C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.588+186C=
ENST00000264896.8:c.612+186C= MANE Select	ENSP00000264896.2:n.612+186C=
ENST00000502908.2:n.2299C=
ENST00000638295.1:c.138+186C=	ENSP00000492288.1:n.138+186C=
ENST00000638372.1:n.864+186C=
ENST00000638603.1:c.612+186C=	ENSP00000491728.1:n.612+186C=
ENST00000638663.1:c.612+186C=	ENSP00000491407.1:n.612+186C=
ENST00000638680.1:n.2193+186C=
ENST00000639145.1:c.603+186C=	ENSP00000492831.1:n.603+186C=
ENST00000639300.1:c.612+186C=	ENSP00000492840.1:n.612+186C=
ENST00000639324.1:n.711+186C=
ENST00000639715.1:c.567+186C=
ENST00000639738.1:c.276-13030C=	ENSP00000491792.1:n.276-13030C=
ENST00000640076.1:n.193+186C=
ENST00000640341.1:c.*252+186C=	ENSP00000492714.1:n.*252+186C=
ENST00000640634.1:c.733+186C=
ENST00000640640.1:c.612+186C=	ENSP00000492246.1:n.612+186C=
ENST00000640957.1:c.612+186C=	ENSP00000492004.1:n.612+186C=
ENST00000264896.6:c.612+186C=	ENSP00000264896.2:n.612+186C=
ENST00000452464.6:c.276-3421C=	ENSP00000399154.2:n.276-3421C=
NM_001204255.1:c.276-3421C=	NP_001191184.1:n.276-3421C=
NM_005506.3:c.612+186C=	NP_005497.1:n.612+186C=
NM_005506.4:c.612+186C= MANE Select	NP_005497.1:n.612+186C=
NM_001204255.2:c.276-3421C=	NP_001191184.1:n.276-3421C=