Canonical Allele Identifier: CA1329111861

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219210709A= , CM000664.2:g.219210709A= GRCh38
NC_000002.11:g.220075431A= , CM000664.1:g.220075431A= GRCh37
NC_000002.10:g.219783675A= NCBI36
NG_032110.1:g.13282T=

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.2256+2T= (ABCB6) MANE Select ENSP00000265316.3:n.2256+2T=
ENST00000295750.5:c.2118+2T= (ABCB6) ENSP00000295750.5:n.2118+2T=
ENST00000265316.7:c.2256+2T= (ABCB6) ENSP00000265316.3:n.2256+2T=
ENST00000295750.4:c.1799+2T= (ABCB6)
ENST00000443805.1:c.244+2T= (ABCB6)
ENST00000446716.5:c.4806+2T= (ATG9A)
ENST00000485773.5:n.290T= (ABCB6)
ENST00000487380.5:n.329+2T= (ABCB6)
ENST00000497882.5:n.2569+2T= (ABCB6)
NM_005689.2:c.2256+2T= (ABCB6) NP_005680.1:n.2256+2T=
NM_001349828.1:c.2118+2T= (ABCB6) NP_001336757.1:n.2118+2T=
NM_005689.3:c.2256+2T= (ABCB6) NP_005680.1:n.2256+2T=
NM_005689.4:c.2256+2T= (ABCB6) MANE Select NP_005680.1:n.2256+2T=
NM_001349828.2:c.2118+2T= (ABCB6) NP_001336757.1:n.2118+2T=