Canonical Allele Identifier: CA2621767769

Gene: SCARB1

Linked Data

• gnomAD v4: 12-124777109-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124777109A>G , CM000674.2:g.124777109A>G	GRCh38
NC_000012.11:g.125261655A>G , CM000674.1:g.125261655A>G	GRCh37
NC_000012.10:g.123827608A>G	NCBI36
NG_028199.1:g.91865T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261693.11:c.*1478T>C MANE Select	ENSP00000261693.6:n.*1478T>C
ENST00000339570.9:c.*1358T>C	ENSP00000343795.4:n.*1358T>C
NM_005505.5:c.*1478T>C MANE Select	NP_005496.4:n.*1478T>C
NM_001082959.2:c.*1358T>C	NP_001076428.1:n.*1358T>C
NM_001367981.1:c.*1470T>C	NP_001354910.1:n.*1470T>C
NM_001367983.1:c.*1478T>C	NP_001354912.1:n.*1478T>C
NM_001367984.1:c.*1478T>C	NP_001354913.1:n.*1478T>C
NM_001367985.1:c.*1478T>C	NP_001354914.1:n.*1478T>C
NM_001367986.1:c.*1478T>C	NP_001354915.1:n.*1478T>C
NM_001367987.1:c.*1358T>C	NP_001354916.1:n.*1358T>C
NM_001367988.1:c.*1478T>C	NP_001354917.1:n.*1478T>C
NM_001367989.1:c.*1489T>C	NP_001354918.1:n.*1489T>C
NR_160416.1:n.3153T>C
NR_160417.1:n.3255T>C
NR_160418.1:n.2714T>C
NR_160419.1:n.3078T>C
NR_160420.1:n.2907T>C
NR_160421.1:n.2830T>C
NR_160422.1:n.3036T>C
NR_160423.1:n.3033T>C
NR_160424.1:n.3018T>C