Canonical Allele Identifier: CA1469489387
Gene: SCARB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76174183G= , CM000666.2:g.76174183G= GRCh38
NC_000004.11:g.77095336G= , CM000666.1:g.77095336G= GRCh37
NC_000004.10:g.77314360G= NCBI36
NG_012054.1:g.44700C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682785.1:n.931C=
ENST00000264896.8:c.955C= MANE Select ENSP00000264896.2:p.Leu319=
ENST00000638295.1:c.481C= ENSP00000492288.1:p.Leu161=
ENST00000638372.1:n.1207C=
ENST00000638409.1:n.1270C=
ENST00000638603.1:c.835C= ENSP00000491728.1:p.Leu279=
ENST00000638663.1:c.955C= ENSP00000491407.1:p.Leu319=
ENST00000638680.1:n.2536C=
ENST00000638843.1:n.948C=
ENST00000639145.1:c.946C= ENSP00000492831.1:p.Leu316=
ENST00000639300.1:c.*242C= ENSP00000492840.1:n.*242C=
ENST00000639715.1:c.910C=
ENST00000639738.1:c.276-7882C= ENSP00000491792.1:n.276-7882C=
ENST00000640076.1:n.536C=
ENST00000640341.1:c.*595C= ENSP00000492714.1:n.*595C=
ENST00000640634.1:c.1076C=
ENST00000640640.1:c.955C= ENSP00000492246.1:p.Leu319=
ENST00000640957.1:c.955C= ENSP00000492004.1:p.Leu319=
ENST00000264896.6:c.955C= ENSP00000264896.2:p.Leu319=
ENST00000452464.6:c.526C= ENSP00000399154.2:p.Leu176=
NM_001204255.1:c.526C= NP_001191184.1:p.Leu176=
NM_005506.3:c.955C= NP_005497.1:p.Leu319=
NM_005506.4:c.955C= MANE Select NP_005497.1:p.Leu319=
NM_001204255.2:c.526C= NP_001191184.1:p.Leu176=