Canonical Allele Identifier: CA2621767680

Gene: SCARB1

Linked Data

• gnomAD v4: 12-124776889-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124776889A>G , CM000674.2:g.124776889A>G	GRCh38
NC_000012.11:g.125261435A>G , CM000674.1:g.125261435A>G	GRCh37
NC_000012.10:g.123827388A>G	NCBI36
NG_028199.1:g.92085T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261693.11:c.*1698T>C MANE Select	ENSP00000261693.6:n.*1698T>C
ENST00000339570.9:c.*1578T>C	ENSP00000343795.4:n.*1578T>C
NM_005505.5:c.*1698T>C MANE Select	NP_005496.4:n.*1698T>C
NM_001082959.2:c.*1578T>C	NP_001076428.1:n.*1578T>C
NM_001367981.1:c.*1690T>C	NP_001354910.1:n.*1690T>C
NM_001367983.1:c.*1698T>C	NP_001354912.1:n.*1698T>C
NM_001367984.1:c.*1698T>C	NP_001354913.1:n.*1698T>C
NM_001367985.1:c.*1698T>C	NP_001354914.1:n.*1698T>C
NM_001367986.1:c.*1698T>C	NP_001354915.1:n.*1698T>C
NM_001367987.1:c.*1578T>C	NP_001354916.1:n.*1578T>C
NM_001367988.1:c.*1698T>C	NP_001354917.1:n.*1698T>C
NM_001367989.1:c.*1709T>C	NP_001354918.1:n.*1709T>C
NR_160416.1:n.3373T>C
NR_160417.1:n.3475T>C
NR_160418.1:n.2934T>C
NR_160419.1:n.3298T>C
NR_160420.1:n.3127T>C
NR_160421.1:n.3050T>C
NR_160422.1:n.3256T>C
NR_160423.1:n.3253T>C
NR_160424.1:n.3238T>C