Canonical Allele Identifier: CA2069464309

Gene: SCARB1

Linked Data

• dbSNP Id: rs1872544783

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124777031T>C , CM000674.2:g.124777031T>C	GRCh38
NC_000012.11:g.125261577T>C , CM000674.1:g.125261577T>C	GRCh37
NC_000012.10:g.123827530T>C	NCBI36
NG_028199.1:g.91943A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261693.11:c.*1556A>G MANE Select	ENSP00000261693.6:n.*1556A>G
ENST00000339570.9:c.*1436A>G	ENSP00000343795.4:n.*1436A>G
NM_005505.5:c.*1556A>G MANE Select	NP_005496.4:n.*1556A>G
NM_001082959.2:c.*1436A>G	NP_001076428.1:n.*1436A>G
NM_001367981.1:c.*1548A>G	NP_001354910.1:n.*1548A>G
NM_001367983.1:c.*1556A>G	NP_001354912.1:n.*1556A>G
NM_001367984.1:c.*1556A>G	NP_001354913.1:n.*1556A>G
NM_001367985.1:c.*1556A>G	NP_001354914.1:n.*1556A>G
NM_001367986.1:c.*1556A>G	NP_001354915.1:n.*1556A>G
NM_001367987.1:c.*1436A>G	NP_001354916.1:n.*1436A>G
NM_001367988.1:c.*1556A>G	NP_001354917.1:n.*1556A>G
NM_001367989.1:c.*1567A>G	NP_001354918.1:n.*1567A>G
NR_160416.1:n.3231A>G
NR_160417.1:n.3333A>G
NR_160418.1:n.2792A>G
NR_160419.1:n.3156A>G
NR_160420.1:n.2985A>G
NR_160421.1:n.2908A>G
NR_160422.1:n.3114A>G
NR_160423.1:n.3111A>G
NR_160424.1:n.3096A>G