Canonical Allele Identifier: CA1469473816

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179372C= , CM000666.2:g.76179372C=	GRCh38
NC_000004.11:g.77100525C= , CM000666.1:g.77100525C=	GRCh37
NC_000004.10:g.77319549C=	NCBI36
NG_012054.1:g.39511G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.588+145G=
ENST00000264896.8:c.612+145G= MANE Select	ENSP00000264896.2:n.612+145G=
ENST00000502908.2:n.2258G=
ENST00000638295.1:c.138+145G=	ENSP00000492288.1:n.138+145G=
ENST00000638372.1:n.864+145G=
ENST00000638603.1:c.612+145G=	ENSP00000491728.1:n.612+145G=
ENST00000638663.1:c.612+145G=	ENSP00000491407.1:n.612+145G=
ENST00000638680.1:n.2193+145G=
ENST00000639145.1:c.603+145G=	ENSP00000492831.1:n.603+145G=
ENST00000639300.1:c.612+145G=	ENSP00000492840.1:n.612+145G=
ENST00000639324.1:n.711+145G=
ENST00000639715.1:c.567+145G=
ENST00000639738.1:c.276-13071G=	ENSP00000491792.1:n.276-13071G=
ENST00000640076.1:n.193+145G=
ENST00000640341.1:c.*252+145G=	ENSP00000492714.1:n.*252+145G=
ENST00000640634.1:c.733+145G=
ENST00000640640.1:c.612+145G=	ENSP00000492246.1:n.612+145G=
ENST00000640916.1:n.685G=
ENST00000640957.1:c.612+145G=	ENSP00000492004.1:n.612+145G=
ENST00000264896.6:c.612+145G=	ENSP00000264896.2:n.612+145G=
ENST00000452464.6:c.276-3462G=	ENSP00000399154.2:n.276-3462G=
NM_001204255.1:c.276-3462G=	NP_001191184.1:n.276-3462G=
NM_005506.3:c.612+145G=	NP_005497.1:n.612+145G=
NM_005506.4:c.612+145G= MANE Select	NP_005497.1:n.612+145G=
NM_001204255.2:c.276-3462G=	NP_001191184.1:n.276-3462G=