Canonical Allele Identifier: CA13657130
Gene: SCARB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4765623

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124836304C>T , CM000674.2:g.124836304C>T GRCh38
NC_000012.10:g.123886803C>T NCBI36
NC_000012.11:g.125320850C>T , CM000674.1:g.125320850C>T GRCh37
NG_028199.1:g.32670G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261693.10:c.127-18597G>A ENSP00000261693.6:p.=
ENST00000339570.9:c.127-18597G>A ENSP00000343795.4:p.=
ENST00000415380.6:c.127-18597G>A ENSP00000414979.2:p.=
ENST00000535005.5:n.442-18597G>A
ENST00000538291.5:n.270-18597G>A
ENST00000539320.2:n.421-18597G>A
ENST00000541661.5:n.168-18597G>A
ENST00000545493.1:c.127-18597G>A ENSP00000443454.1:p.=
ENST00000546215.5:c.127-18597G>A ENSP00000442862.1:p.=
NM_001082959.1:c.127-18597G>A NP_001076428.1:p.=
NM_005505.4:c.127-18597G>A NP_005496.4:p.=