Canonical Allele Identifier: CA1329111858

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219210706C= , CM000664.2:g.219210706C= GRCh38
NC_000002.11:g.220075428C= , CM000664.1:g.220075428C= GRCh37
NC_000002.10:g.219783672C= NCBI36
NG_032110.1:g.13285G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.2256+5G= (ABCB6) MANE Select ENSP00000265316.3:n.2256+5G=
ENST00000295750.5:c.2118+5G= (ABCB6) ENSP00000295750.5:n.2118+5G=
ENST00000265316.7:c.2256+5G= (ABCB6) ENSP00000265316.3:n.2256+5G=
ENST00000295750.4:c.1799+5G= (ABCB6)
ENST00000443805.1:c.244+5G= (ABCB6)
ENST00000446716.5:c.4806+5G= (ATG9A)
ENST00000485773.5:n.293G= (ABCB6)
ENST00000487380.5:n.329+5G= (ABCB6)
ENST00000497882.5:n.2569+5G= (ABCB6)
NM_005689.2:c.2256+5G= (ABCB6) NP_005680.1:n.2256+5G=
NM_001349828.1:c.2118+5G= (ABCB6) NP_001336757.1:n.2118+5G=
NM_005689.3:c.2256+5G= (ABCB6) NP_005680.1:n.2256+5G=
NM_005689.4:c.2256+5G= (ABCB6) MANE Select NP_005680.1:n.2256+5G=
NM_001349828.2:c.2118+5G= (ABCB6) NP_001336757.1:n.2118+5G=