Canonical Allele Identifier: CA2970288

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76176432C>T , CM000666.2:g.76176432C>T	GRCh38
NC_000004.11:g.77097585C>T , CM000666.1:g.77097585C>T	GRCh37
NC_000004.10:g.77316609C>T	NCBI36
NG_012054.1:g.42451G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005506.4:c.704+5G>A MANE Select	NP_005497.1:n.704+5G>A
ENST00000264896.8:c.704+5G>A MANE Select	ENSP00000264896.2:n.704+5G>A
NM_001204255.1:c.276-522G>A	NP_001191184.1:n.276-522G>A
NM_001204255.2:c.276-522G>A	NP_001191184.1:n.276-522G>A
NM_005506.3:c.704+5G>A	NP_005497.1:n.704+5G>A
ENST00000264896.6:c.704+5G>A	ENSP00000264896.2:n.704+5G>A
ENST00000452464.6:c.276-522G>A	ENSP00000399154.2:n.276-522G>A
ENST00000638295.1:c.230+5G>A	ENSP00000492288.1:n.230+5G>A
ENST00000638372.1:n.956+5G>A
ENST00000638603.1:c.704+5G>A	ENSP00000491728.1:n.704+5G>A
ENST00000638663.1:c.704+5G>A	ENSP00000491407.1:n.704+5G>A
ENST00000638680.1:n.2285+5G>A
ENST00000638843.1:n.697+5G>A
ENST00000639145.1:c.695+5G>A	ENSP00000492831.1:n.695+5G>A
ENST00000639300.1:c.613-522G>A	ENSP00000492840.1:n.613-522G>A
ENST00000639324.1:n.803+5G>A
ENST00000639715.1:c.659+5G>A
ENST00000639738.1:c.276-10131G>A	ENSP00000491792.1:n.276-10131G>A
ENST00000640076.1:n.285+5G>A
ENST00000640341.1:c.*344+5G>A	ENSP00000492714.1:n.*344+5G>A
ENST00000640634.1:c.825+5G>A
ENST00000640640.1:c.704+5G>A	ENSP00000492246.1:n.704+5G>A
ENST00000640957.1:c.704+5G>A	ENSP00000492004.1:n.704+5G>A
ENST00000682785.1:n.680+5G>A