Canonical Allele Identifier: CA2970438

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76213520C>T , CM000666.2:g.76213520C>T	GRCh38
NC_000004.11:g.77134673C>T , CM000666.1:g.77134673C>T	GRCh37
NC_000004.10:g.77353697C>T	NCBI36
NG_012054.1:g.5363G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005506.4:c.24G>A MANE Select	NP_005497.1:p.Thr8=
ENST00000264896.8:c.24G>A MANE Select	ENSP00000264896.2:p.Thr8=
NM_001204255.1:c.24G>A	NP_001191184.1:p.Thr8=
NM_001204255.2:c.24G>A	NP_001191184.1:p.Thr8=
NM_005506.3:c.24G>A	NP_005497.1:p.Thr8=
ENST00000264896.6:c.24G>A	ENSP00000264896.2:p.Thr8=
ENST00000452464.6:c.24G>A	ENSP00000399154.2:p.Thr8=
ENST00000502908.2:n.277G>A
ENST00000509994.1:c.24G>A	ENSP00000420988.1:p.Thr8=
ENST00000509994.2:c.24G>A	ENSP00000420988.1:p.Thr8=
ENST00000638295.1:c.-357-17656G>A	ENSP00000492288.1:n.-357-17656G>A
ENST00000638372.1:n.276G>A
ENST00000638567.1:n.307G>A
ENST00000638603.1:c.24G>A	ENSP00000491728.1:p.Thr8=
ENST00000638663.1:c.24G>A	ENSP00000491407.1:p.Thr8=
ENST00000638680.1:n.357G>A
ENST00000639145.1:c.24G>A	ENSP00000492831.1:p.Thr8=
ENST00000639300.1:c.24G>A	ENSP00000492840.1:p.Thr8=
ENST00000639738.1:c.24G>A	ENSP00000491792.1:p.Thr8=
ENST00000640341.1:c.24G>A	ENSP00000492714.1:p.Thr8=
ENST00000640634.1:c.1G>A
ENST00000640640.1:c.24G>A	ENSP00000492246.1:p.Thr8=
ENST00000640957.1:c.24G>A	ENSP00000492004.1:p.Thr8=