Canonical Allele Identifier: CA11907452

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76176605T>C , CM000666.2:g.76176605T>C	GRCh38
NC_000004.11:g.77097758T>C , CM000666.1:g.77097758T>C	GRCh37
NC_000004.10:g.77316782T>C	NCBI36
NG_012054.1:g.42278A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.589-77A>G
ENST00000264896.8:c.613-77A>G MANE Select	ENSP00000264896.2:n.613-77A>G
ENST00000638295.1:c.139-77A>G	ENSP00000492288.1:n.139-77A>G
ENST00000638372.1:n.865-77A>G
ENST00000638603.1:c.613-77A>G	ENSP00000491728.1:n.613-77A>G
ENST00000638663.1:c.613-77A>G	ENSP00000491407.1:n.613-77A>G
ENST00000638680.1:n.2194-77A>G
ENST00000638843.1:n.529A>G
ENST00000639145.1:c.604-77A>G	ENSP00000492831.1:n.604-77A>G
ENST00000639300.1:c.613-695A>G	ENSP00000492840.1:n.613-695A>G
ENST00000639324.1:n.712-77A>G
ENST00000639715.1:c.568-77A>G
ENST00000639738.1:c.276-10304A>G	ENSP00000491792.1:n.276-10304A>G
ENST00000640076.1:n.194-77A>G
ENST00000640341.1:c.*253-77A>G	ENSP00000492714.1:n.*253-77A>G
ENST00000640634.1:c.734-77A>G
ENST00000640640.1:c.613-77A>G	ENSP00000492246.1:n.613-77A>G
ENST00000640957.1:c.613-77A>G	ENSP00000492004.1:n.613-77A>G
ENST00000264896.6:c.613-77A>G	ENSP00000264896.2:n.613-77A>G
ENST00000452464.6:c.276-695A>G	ENSP00000399154.2:n.276-695A>G
NM_001204255.1:c.276-695A>G	NP_001191184.1:n.276-695A>G
NM_005506.3:c.613-77A>G	NP_005497.1:n.613-77A>G
NM_005506.4:c.613-77A>G MANE Select	NP_005497.1:n.613-77A>G
NM_001204255.2:c.276-695A>G	NP_001191184.1:n.276-695A>G