Canonical Allele Identifier: CA1469474131

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179563T= , CM000666.2:g.76179563T=	GRCh38
NC_000004.11:g.77100716T= , CM000666.1:g.77100716T=	GRCh37
NC_000004.10:g.77319740T=	NCBI36
NG_012054.1:g.39320A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.542A=
ENST00000264896.8:c.566A= MANE Select	ENSP00000264896.2:p.His189=
ENST00000502908.2:n.2067A=
ENST00000638295.1:c.92A=	ENSP00000492288.1:p.His31=
ENST00000638372.1:n.818A=
ENST00000638603.1:c.566A=	ENSP00000491728.1:p.His189=
ENST00000638663.1:c.566A=	ENSP00000491407.1:p.His189=
ENST00000638680.1:n.2147A=
ENST00000639145.1:c.557A=	ENSP00000492831.1:p.His186=
ENST00000639300.1:c.566A=	ENSP00000492840.1:p.His189=
ENST00000639324.1:n.665A=
ENST00000639715.1:c.521A=
ENST00000639738.1:c.276-13262A=	ENSP00000491792.1:n.276-13262A=
ENST00000640076.1:n.147A=
ENST00000640341.1:c.*206A=	ENSP00000492714.1:n.*206A=
ENST00000640634.1:c.687A=
ENST00000640640.1:c.566A=	ENSP00000492246.1:p.His189=
ENST00000640916.1:n.494A=
ENST00000640957.1:c.566A=	ENSP00000492004.1:p.His189=
ENST00000264896.6:c.566A=	ENSP00000264896.2:p.His189=
ENST00000452464.6:c.276-3653A=	ENSP00000399154.2:n.276-3653A=
NM_001204255.1:c.276-3653A=	NP_001191184.1:n.276-3653A=
NM_005506.3:c.566A=	NP_005497.1:p.His189=
NM_005506.4:c.566A= MANE Select	NP_005497.1:p.His189=
NM_001204255.2:c.276-3653A=	NP_001191184.1:n.276-3653A=