Canonical Allele Identifier: CA350635118

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219213842G>T , CM000664.2:g.219213842G>T GRCh38
NC_000002.11:g.220078564G>T , CM000664.1:g.220078564G>T GRCh37
NC_000002.10:g.219786808G>T NCBI36
NG_032110.1:g.10149C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.1562C>A (ABCB6) MANE Select ENSP00000265316.3:p.Thr521Asn
ENST00000295750.5:c.1424C>A (ABCB6) ENSP00000295750.5:p.Thr475Asn
ENST00000265316.7:c.1562C>A (ABCB6) ENSP00000265316.3:p.Thr521Asn
ENST00000295750.4:c.1105C>A (ABCB6)
ENST00000446716.5:c.4287C>A (ATG9A)
ENST00000448398.5:c.638C>A (ABCB6)
ENST00000494639.5:n.471C>A (ABCB6)
ENST00000497882.5:n.1875C>A (ABCB6)
NM_005689.2:c.1562C>A (ABCB6) NP_005680.1:p.Thr521Asn
NM_001349828.1:c.1424C>A (ABCB6) NP_001336757.1:p.Thr475Asn
NM_005689.3:c.1562C>A (ABCB6) NP_005680.1:p.Thr521Asn
NM_005689.4:c.1562C>A (ABCB6) MANE Select NP_005680.1:p.Thr521Asn
NM_001349828.2:c.1424C>A (ABCB6) NP_001336757.1:p.Thr475Asn