Canonical Allele Identifier: CA1329111853

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219210699C= , CM000664.2:g.219210699C= GRCh38
NC_000002.11:g.220075421C= , CM000664.1:g.220075421C= GRCh37
NC_000002.10:g.219783665C= NCBI36
NG_032110.1:g.13292G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.2256+12G= (ABCB6) MANE Select ENSP00000265316.3:n.2256+12G=
ENST00000295750.5:c.2118+12G= (ABCB6) ENSP00000295750.5:n.2118+12G=
ENST00000265316.7:c.2256+12G= (ABCB6) ENSP00000265316.3:n.2256+12G=
ENST00000295750.4:c.1799+12G= (ABCB6)
ENST00000443805.1:c.244+12G= (ABCB6)
ENST00000446716.5:c.4806+12G= (ATG9A)
ENST00000485773.5:n.300G= (ABCB6)
ENST00000487380.5:n.329+12G= (ABCB6)
ENST00000497882.5:n.2569+12G= (ABCB6)
NM_005689.2:c.2256+12G= (ABCB6) NP_005680.1:n.2256+12G=
NM_001349828.1:c.2118+12G= (ABCB6) NP_001336757.1:n.2118+12G=
NM_005689.3:c.2256+12G= (ABCB6) NP_005680.1:n.2256+12G=
NM_005689.4:c.2256+12G= (ABCB6) MANE Select NP_005680.1:n.2256+12G=
NM_001349828.2:c.2118+12G= (ABCB6) NP_001336757.1:n.2118+12G=