Canonical Allele Identifier: CA2573138361

Gene: SCARB2

Linked Data

• ClinVar Variation Id: 1552331
• ClinVar RCV Id: RCV002196995
• dbSNP Id: rs2109947094

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179502G>C , CM000666.2:g.76179502G>C	GRCh38
NC_000004.11:g.77100655G>C , CM000666.1:g.77100655G>C	GRCh37
NC_000004.10:g.77319679G>C	NCBI36
NG_012054.1:g.39381C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.588+15C>G
ENST00000264896.8:c.612+15C>G MANE Select	ENSP00000264896.2:n.612+15C>G
ENST00000502908.2:n.2128C>G
ENST00000638295.1:c.138+15C>G	ENSP00000492288.1:n.138+15C>G
ENST00000638372.1:n.864+15C>G
ENST00000638603.1:c.612+15C>G	ENSP00000491728.1:n.612+15C>G
ENST00000638663.1:c.612+15C>G	ENSP00000491407.1:n.612+15C>G
ENST00000638680.1:n.2193+15C>G
ENST00000639145.1:c.603+15C>G	ENSP00000492831.1:n.603+15C>G
ENST00000639300.1:c.612+15C>G	ENSP00000492840.1:n.612+15C>G
ENST00000639324.1:n.711+15C>G
ENST00000639715.1:c.567+15C>G
ENST00000639738.1:c.276-13201C>G	ENSP00000491792.1:n.276-13201C>G
ENST00000640076.1:n.193+15C>G
ENST00000640341.1:c.*252+15C>G	ENSP00000492714.1:n.*252+15C>G
ENST00000640634.1:c.733+15C>G
ENST00000640640.1:c.612+15C>G	ENSP00000492246.1:n.612+15C>G
ENST00000640916.1:n.555C>G
ENST00000640957.1:c.612+15C>G	ENSP00000492004.1:n.612+15C>G
ENST00000264896.6:c.612+15C>G	ENSP00000264896.2:n.612+15C>G
ENST00000452464.6:c.276-3592C>G	ENSP00000399154.2:n.276-3592C>G
NM_001204255.1:c.276-3592C>G	NP_001191184.1:n.276-3592C>G
NM_005506.3:c.612+15C>G	NP_005497.1:n.612+15C>G
NM_005506.4:c.612+15C>G MANE Select	NP_005497.1:n.612+15C>G
NM_001204255.2:c.276-3592C>G	NP_001191184.1:n.276-3592C>G