Canonical Allele Identifier: CA350682708

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219210713C>A , CM000664.2:g.219210713C>A GRCh38
NC_000002.11:g.220075435C>A , CM000664.1:g.220075435C>A GRCh37
NC_000002.10:g.219783679C>A NCBI36
NG_032110.1:g.13278G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.2254G>T (ABCB6) MANE Select ENSP00000265316.3:p.Glu752Ter
ENST00000295750.5:c.2116G>T (ABCB6) ENSP00000295750.5:p.Glu706Ter
ENST00000265316.7:c.2254G>T (ABCB6) ENSP00000265316.3:p.Glu752Ter
ENST00000295750.4:c.1797G>T (ABCB6)
ENST00000443805.1:c.242G>T (ABCB6)
ENST00000446716.5:c.4804G>T (ATG9A)
ENST00000485773.5:n.286G>T (ABCB6)
ENST00000487380.5:n.327G>T (ABCB6)
ENST00000492543.1:n.804G>T (ABCB6)
ENST00000497882.5:n.2567G>T (ABCB6)
NM_005689.2:c.2254G>T (ABCB6) NP_005680.1:p.Glu752Ter
NM_001349828.1:c.2116G>T (ABCB6) NP_001336757.1:p.Glu706Ter
NM_005689.3:c.2254G>T (ABCB6) NP_005680.1:p.Glu752Ter
NM_005689.4:c.2254G>T (ABCB6) MANE Select NP_005680.1:p.Glu752Ter
NM_001349828.2:c.2116G>T (ABCB6) NP_001336757.1:p.Glu706Ter