Canonical Allele Identifier: CA357326925

Gene: SCARB2

Linked Data

• MyVariant Identifiers: chr4:g.77100797G>C (hg19) ; chr4:g.76179644G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179644G>C , CM000666.2:g.76179644G>C	GRCh38
NC_000004.11:g.77100797G>C , CM000666.1:g.77100797G>C	GRCh37
NC_000004.10:g.77319821G>C	NCBI36
NG_012054.1:g.39239C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.461C>G
ENST00000264896.8:c.485C>G MANE Select	ENSP00000264896.2:p.Ala162Gly
ENST00000502908.2:n.1986C>G
ENST00000638295.1:c.11C>G	ENSP00000492288.1:p.Ala4Gly
ENST00000638372.1:n.737C>G
ENST00000638603.1:c.485C>G	ENSP00000491728.1:p.Ala162Gly
ENST00000638663.1:c.485C>G	ENSP00000491407.1:p.Ala162Gly
ENST00000638680.1:n.2066C>G
ENST00000639145.1:c.476C>G	ENSP00000492831.1:p.Ala159Gly
ENST00000639300.1:c.485C>G	ENSP00000492840.1:p.Ala162Gly
ENST00000639324.1:n.584C>G
ENST00000639715.1:c.440C>G
ENST00000639738.1:c.276-13343C>G	ENSP00000491792.1:n.276-13343C>G
ENST00000640076.1:n.66C>G
ENST00000640341.1:c.*125C>G	ENSP00000492714.1:n.*125C>G
ENST00000640634.1:c.606C>G
ENST00000640640.1:c.485C>G	ENSP00000492246.1:p.Ala162Gly
ENST00000640916.1:n.413C>G
ENST00000640957.1:c.485C>G	ENSP00000492004.1:p.Ala162Gly
ENST00000264896.6:c.485C>G	ENSP00000264896.2:p.Ala162Gly
ENST00000452464.6:c.276-3734C>G	ENSP00000399154.2:n.276-3734C>G
NM_001204255.1:c.276-3734C>G	NP_001191184.1:n.276-3734C>G
NM_005506.3:c.485C>G	NP_005497.1:p.Ala162Gly
NM_005506.4:c.485C>G MANE Select	NP_005497.1:p.Ala162Gly
NM_001204255.2:c.276-3734C>G	NP_001191184.1:n.276-3734C>G