Canonical Allele Identifier: CA2621767677

Gene: SCARB1

Linked Data

• gnomAD v4: 12-124776886-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124776886G>T , CM000674.2:g.124776886G>T	GRCh38
NC_000012.11:g.125261432G>T , CM000674.1:g.125261432G>T	GRCh37
NC_000012.10:g.123827385G>T	NCBI36
NG_028199.1:g.92088C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261693.11:c.*1701C>A MANE Select	ENSP00000261693.6:n.*1701C>A
ENST00000339570.9:c.*1581C>A	ENSP00000343795.4:n.*1581C>A
NM_005505.5:c.*1701C>A MANE Select	NP_005496.4:n.*1701C>A
NM_001082959.2:c.*1581C>A	NP_001076428.1:n.*1581C>A
NM_001367981.1:c.*1693C>A	NP_001354910.1:n.*1693C>A
NM_001367983.1:c.*1701C>A	NP_001354912.1:n.*1701C>A
NM_001367984.1:c.*1701C>A	NP_001354913.1:n.*1701C>A
NM_001367985.1:c.*1701C>A	NP_001354914.1:n.*1701C>A
NM_001367986.1:c.*1701C>A	NP_001354915.1:n.*1701C>A
NM_001367987.1:c.*1581C>A	NP_001354916.1:n.*1581C>A
NM_001367988.1:c.*1701C>A	NP_001354917.1:n.*1701C>A
NM_001367989.1:c.*1712C>A	NP_001354918.1:n.*1712C>A
NR_160416.1:n.3376C>A
NR_160417.1:n.3478C>A
NR_160418.1:n.2937C>A
NR_160419.1:n.3301C>A
NR_160420.1:n.3130C>A
NR_160421.1:n.3053C>A
NR_160422.1:n.3259C>A
NR_160423.1:n.3256C>A
NR_160424.1:n.3241C>A