Canonical Allele Identifier: CA13657105
Gene: SCARB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11057820

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124812418C>T , CM000674.2:g.124812418C>T GRCh38
NC_000012.11:g.125296964C>T , CM000674.1:g.125296964C>T GRCh37
NC_000012.10:g.123862917C>T NCBI36
NG_028199.1:g.56556G>A

Transcript Alleles

HGVS Amino-acid change
NM_001082959.1:c.631-453G>A VV NP_001076428.1:p.=
NM_005505.4:c.631-453G>A VV NP_005496.4:p.=
NM_005505.5:c.631-453G>A VV MANE Preferred NP_005496.4:p.=
ENST00000261693.10:c.631-453G>A ENSP00000261693.6:p.=
ENST00000339570.9:c.631-453G>A ENSP00000343795.4:p.=
ENST00000415380.6:c.631-453G>A ENSP00000414979.2:p.=
ENST00000535005.5:n.946-453G>A
ENST00000538291.5:n.774-453G>A
ENST00000544327.1:c.469-453G>A ENSP00000444851.1:p.=
ENST00000546215.5:c.631-453G>A ENSP00000442862.1:p.=