Canonical Allele Identifier: CA1469489395
Gene: SCARB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76174187G= , CM000666.2:g.76174187G= GRCh38
NC_000004.11:g.77095340G= , CM000666.1:g.77095340G= GRCh37
NC_000004.10:g.77314364G= NCBI36
NG_012054.1:g.44696C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682785.1:n.927C=
ENST00000264896.8:c.951C= MANE Select ENSP00000264896.2:p.Asn317=
ENST00000638295.1:c.477C= ENSP00000492288.1:p.Asn159=
ENST00000638372.1:n.1203C=
ENST00000638409.1:n.1266C=
ENST00000638603.1:c.831C= ENSP00000491728.1:p.Asn277=
ENST00000638663.1:c.951C= ENSP00000491407.1:p.Asn317=
ENST00000638680.1:n.2532C=
ENST00000638843.1:n.944C=
ENST00000639145.1:c.942C= ENSP00000492831.1:p.Asn314=
ENST00000639300.1:c.*238C= ENSP00000492840.1:n.*238C=
ENST00000639715.1:c.906C=
ENST00000639738.1:c.276-7886C= ENSP00000491792.1:n.276-7886C=
ENST00000640076.1:n.532C=
ENST00000640341.1:c.*591C= ENSP00000492714.1:n.*591C=
ENST00000640634.1:c.1072C=
ENST00000640640.1:c.951C= ENSP00000492246.1:p.Asn317=
ENST00000640957.1:c.951C= ENSP00000492004.1:p.Asn317=
ENST00000264896.6:c.951C= ENSP00000264896.2:p.Asn317=
ENST00000452464.6:c.522C= ENSP00000399154.2:p.Asn174=
NM_001204255.1:c.522C= NP_001191184.1:p.Asn174=
NM_005506.3:c.951C= NP_005497.1:p.Asn317=
NM_005506.4:c.951C= MANE Select NP_005497.1:p.Asn317=
NM_001204255.2:c.522C= NP_001191184.1:p.Asn174=