Canonical Allele Identifier: CA1469474336

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179643G= , CM000666.2:g.76179643G=	GRCh38
NC_000004.11:g.77100796G= , CM000666.1:g.77100796G=	GRCh37
NC_000004.10:g.77319820G=	NCBI36
NG_012054.1:g.39240C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.462C=
ENST00000264896.8:c.486C= MANE Select	ENSP00000264896.2:p.Ala162=
ENST00000502908.2:n.1987C=
ENST00000638295.1:c.12C=	ENSP00000492288.1:p.Ala4=
ENST00000638372.1:n.738C=
ENST00000638603.1:c.486C=	ENSP00000491728.1:p.Ala162=
ENST00000638663.1:c.486C=	ENSP00000491407.1:p.Ala162=
ENST00000638680.1:n.2067C=
ENST00000639145.1:c.477C=	ENSP00000492831.1:p.Ala159=
ENST00000639300.1:c.486C=	ENSP00000492840.1:p.Ala162=
ENST00000639324.1:n.585C=
ENST00000639715.1:c.441C=
ENST00000639738.1:c.276-13342C=	ENSP00000491792.1:n.276-13342C=
ENST00000640076.1:n.67C=
ENST00000640341.1:c.*126C=	ENSP00000492714.1:n.*126C=
ENST00000640634.1:c.607C=
ENST00000640640.1:c.486C=	ENSP00000492246.1:p.Ala162=
ENST00000640916.1:n.414C=
ENST00000640957.1:c.486C=	ENSP00000492004.1:p.Ala162=
ENST00000264896.6:c.486C=	ENSP00000264896.2:p.Ala162=
ENST00000452464.6:c.276-3733C=	ENSP00000399154.2:n.276-3733C=
NM_001204255.1:c.276-3733C=	NP_001191184.1:n.276-3733C=
NM_005506.3:c.486C=	NP_005497.1:p.Ala162=
NM_005506.4:c.486C= MANE Select	NP_005497.1:p.Ala162=
NM_001204255.2:c.276-3733C=	NP_001191184.1:n.276-3733C=