Canonical Allele Identifier: CA439953789
Gene: SCARB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.77100721A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76179568A>T , CM000666.2:g.76179568A>T GRCh38
NC_000004.11:g.77100721A>T , CM000666.1:g.77100721A>T GRCh37
NC_000004.10:g.77319745A>T NCBI36
NG_012054.1:g.39315T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682785.1:n.537T>A
ENST00000264896.8:c.561T>A MANE Select ENSP00000264896.2:p.Leu187=
ENST00000502908.2:n.2062T>A
ENST00000638295.1:c.87T>A ENSP00000492288.1:p.Leu29=
ENST00000638372.1:n.813T>A
ENST00000638603.1:c.561T>A ENSP00000491728.1:p.Leu187=
ENST00000638663.1:c.561T>A ENSP00000491407.1:p.Leu187=
ENST00000638680.1:n.2142T>A
ENST00000639145.1:c.552T>A ENSP00000492831.1:p.Leu184=
ENST00000639300.1:c.561T>A ENSP00000492840.1:p.Leu187=
ENST00000639324.1:n.660T>A
ENST00000639715.1:c.516T>A
ENST00000639738.1:c.276-13267T>A ENSP00000491792.1:n.276-13267T>A
ENST00000640076.1:n.142T>A
ENST00000640341.1:c.*201T>A ENSP00000492714.1:n.*201T>A
ENST00000640634.1:c.682T>A
ENST00000640640.1:c.561T>A ENSP00000492246.1:p.Leu187=
ENST00000640916.1:n.489T>A
ENST00000640957.1:c.561T>A ENSP00000492004.1:p.Leu187=
ENST00000264896.6:c.561T>A ENSP00000264896.2:p.Leu187=
ENST00000452464.6:c.276-3658T>A ENSP00000399154.2:n.276-3658T>A
NM_001204255.1:c.276-3658T>A NP_001191184.1:n.276-3658T>A
NM_005506.3:c.561T>A NP_005497.1:p.Leu187=
NM_005506.4:c.561T>A MANE Select NP_005497.1:p.Leu187=
NM_001204255.2:c.276-3658T>A NP_001191184.1:n.276-3658T>A