Canonical Allele Identifier: CA99884585
Gene: SCARB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76162031G>A , CM000666.2:g.76162031G>A GRCh38
NC_000004.11:g.77083184G>A , CM000666.1:g.77083184G>A GRCh37
NC_000004.10:g.77302208G>A NCBI36
NG_012054.1:g.56852C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682785.1:n.1375-280C>T
ENST00000264896.8:c.1399-280C>T MANE Select ENSP00000264896.2:n.1399-280C>T
ENST00000511129.2:n.775-280C>T
ENST00000638295.1:c.925-280C>T ENSP00000492288.1:n.925-280C>T
ENST00000638372.1:n.4517-280C>T
ENST00000638603.1:c.1279-280C>T ENSP00000491728.1:n.1279-280C>T
ENST00000638663.1:c.*181-280C>T ENSP00000491407.1:n.*181-280C>T
ENST00000638680.1:n.2980-280C>T
ENST00000639145.1:c.1390-280C>T ENSP00000492831.1:n.1390-280C>T
ENST00000639300.1:c.*686-280C>T ENSP00000492840.1:n.*686-280C>T
ENST00000639715.1:c.1354-280C>T
ENST00000639738.1:c.487-280C>T ENSP00000491792.1:n.487-280C>T
ENST00000640341.1:c.*1039-280C>T ENSP00000492714.1:n.*1039-280C>T
ENST00000640634.1:c.1520-280C>T
ENST00000640640.1:c.1337-280C>T ENSP00000492246.1:n.1337-280C>T
ENST00000640880.1:c.212-287C>T
ENST00000640900.1:n.234-280C>T
ENST00000640957.1:c.*1179C>T ENSP00000492004.1:n.*1179C>T
ENST00000264896.6:c.1399-280C>T ENSP00000264896.2:n.1399-280C>T
ENST00000452464.6:c.970-280C>T ENSP00000399154.2:n.970-280C>T
NM_001204255.1:c.970-280C>T NP_001191184.1:n.970-280C>T
NM_005506.3:c.1399-280C>T NP_005497.1:n.1399-280C>T
NM_005506.4:c.1399-280C>T MANE Select NP_005497.1:n.1399-280C>T
NM_001204255.2:c.970-280C>T NP_001191184.1:n.970-280C>T