Canonical Allele Identifier: CA2671071078
Gene: SCARB2 HGNC NCBI

Linked Data

gnomAD v4: 4-76179404-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76179404A>T , CM000666.2:g.76179404A>T GRCh38
NC_000004.11:g.77100557A>T , CM000666.1:g.77100557A>T GRCh37
NC_000004.10:g.77319581A>T NCBI36
NG_012054.1:g.39479T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682785.1:n.588+113T>A
ENST00000264896.8:c.612+113T>A MANE Select ENSP00000264896.2:n.612+113T>A
ENST00000502908.2:n.2226T>A
ENST00000638295.1:c.138+113T>A ENSP00000492288.1:n.138+113T>A
ENST00000638372.1:n.864+113T>A
ENST00000638603.1:c.612+113T>A ENSP00000491728.1:n.612+113T>A
ENST00000638663.1:c.612+113T>A ENSP00000491407.1:n.612+113T>A
ENST00000638680.1:n.2193+113T>A
ENST00000639145.1:c.603+113T>A ENSP00000492831.1:n.603+113T>A
ENST00000639300.1:c.612+113T>A ENSP00000492840.1:n.612+113T>A
ENST00000639324.1:n.711+113T>A
ENST00000639715.1:c.567+113T>A
ENST00000639738.1:c.276-13103T>A ENSP00000491792.1:n.276-13103T>A
ENST00000640076.1:n.193+113T>A
ENST00000640341.1:c.*252+113T>A ENSP00000492714.1:n.*252+113T>A
ENST00000640634.1:c.733+113T>A
ENST00000640640.1:c.612+113T>A ENSP00000492246.1:n.612+113T>A
ENST00000640916.1:n.653T>A
ENST00000640957.1:c.612+113T>A ENSP00000492004.1:n.612+113T>A
ENST00000264896.6:c.612+113T>A ENSP00000264896.2:n.612+113T>A
ENST00000452464.6:c.276-3494T>A ENSP00000399154.2:n.276-3494T>A
NM_001204255.1:c.276-3494T>A NP_001191184.1:n.276-3494T>A
NM_005506.3:c.612+113T>A NP_005497.1:n.612+113T>A
NM_005506.4:c.612+113T>A MANE Select NP_005497.1:n.612+113T>A
NM_001204255.2:c.276-3494T>A NP_001191184.1:n.276-3494T>A