Canonical Allele Identifier: CA357326883
Community Standard Title: NM_005506.4(SCARB2):c.502T>C (p.Phe168Leu)
Gene: SCARB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76179627A>G , CM000666.2:g.76179627A>G GRCh38
NC_000004.11:g.77100780A>G , CM000666.1:g.77100780A>G GRCh37
NC_000004.10:g.77319804A>G NCBI36
NG_012054.1:g.39256T>C

Transcript Alleles

HGVS Amino-acid Change
NM_005506.4:c.502T>C MANE Select NP_005497.1:p.Phe168Leu
ENST00000264896.8:c.502T>C MANE Select ENSP00000264896.2:p.Phe168Leu
NM_001204255.1:c.276-3717T>C NP_001191184.1:n.276-3717T>C
NM_001204255.2:c.276-3717T>C NP_001191184.1:n.276-3717T>C
NM_005506.3:c.502T>C NP_005497.1:p.Phe168Leu
ENST00000264896.6:c.502T>C ENSP00000264896.2:p.Phe168Leu
ENST00000452464.6:c.276-3717T>C ENSP00000399154.2:n.276-3717T>C
ENST00000502908.2:n.2003T>C
ENST00000638295.1:c.28T>C ENSP00000492288.1:p.Phe10Leu
ENST00000638372.1:n.754T>C
ENST00000638603.1:c.502T>C ENSP00000491728.1:p.Phe168Leu
ENST00000638663.1:c.502T>C ENSP00000491407.1:p.Phe168Leu
ENST00000638680.1:n.2083T>C
ENST00000639145.1:c.493T>C ENSP00000492831.1:p.Phe165Leu
ENST00000639300.1:c.502T>C ENSP00000492840.1:p.Phe168Leu
ENST00000639324.1:n.601T>C
ENST00000639715.1:c.457T>C
ENST00000639738.1:c.276-13326T>C ENSP00000491792.1:n.276-13326T>C
ENST00000640076.1:n.83T>C
ENST00000640341.1:c.*142T>C ENSP00000492714.1:n.*142T>C
ENST00000640634.1:c.623T>C
ENST00000640640.1:c.502T>C ENSP00000492246.1:p.Phe168Leu
ENST00000640916.1:n.430T>C
ENST00000640957.1:c.502T>C ENSP00000492004.1:p.Phe168Leu
ENST00000682785.1:n.478T>C