Canonical Allele Identifier: CA1469489569
Gene: SCARB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76174276G= , CM000666.2:g.76174276G= GRCh38
NC_000004.11:g.77095429G= , CM000666.1:g.77095429G= GRCh37
NC_000004.10:g.77314453G= NCBI36
NG_012054.1:g.44607C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682785.1:n.838C=
ENST00000264896.8:c.862C= MANE Select ENSP00000264896.2:p.Gln288=
ENST00000638175.1:n.499C=
ENST00000638295.1:c.388C= ENSP00000492288.1:p.Gln130=
ENST00000638372.1:n.1114C=
ENST00000638409.1:n.1177C=
ENST00000638603.1:c.742C= ENSP00000491728.1:p.Gln248=
ENST00000638663.1:c.862C= ENSP00000491407.1:p.Gln288=
ENST00000638680.1:n.2443C=
ENST00000638843.1:n.855C=
ENST00000639145.1:c.853C= ENSP00000492831.1:p.Gln285=
ENST00000639300.1:c.*149C= ENSP00000492840.1:n.*149C=
ENST00000639715.1:c.817C=
ENST00000639738.1:c.276-7975C= ENSP00000491792.1:n.276-7975C=
ENST00000640076.1:n.443C=
ENST00000640341.1:c.*502C= ENSP00000492714.1:n.*502C=
ENST00000640634.1:c.983C=
ENST00000640640.1:c.862C= ENSP00000492246.1:p.Gln288=
ENST00000640957.1:c.862C= ENSP00000492004.1:p.Gln288=
ENST00000264896.6:c.862C= ENSP00000264896.2:p.Gln288=
ENST00000452464.6:c.433C= ENSP00000399154.2:p.Gln145=
NM_001204255.1:c.433C= NP_001191184.1:p.Gln145=
NM_005506.3:c.862C= NP_005497.1:p.Gln288=
NM_005506.4:c.862C= MANE Select NP_005497.1:p.Gln288=
NM_001204255.2:c.433C= NP_001191184.1:p.Gln145=