Canonical Allele Identifier: CA350635091

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219213836T>G , CM000664.2:g.219213836T>G GRCh38
NC_000002.11:g.220078558T>G , CM000664.1:g.220078558T>G GRCh37
NC_000002.10:g.219786802T>G NCBI36
NG_032110.1:g.10155A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.1568A>C (ABCB6) MANE Select ENSP00000265316.3:p.Gln523Pro
ENST00000295750.5:c.1430A>C (ABCB6) ENSP00000295750.5:p.Gln477Pro
ENST00000265316.7:c.1568A>C (ABCB6) ENSP00000265316.3:p.Gln523Pro
ENST00000295750.4:c.1111A>C (ABCB6)
ENST00000446716.5:c.4293A>C (ATG9A)
ENST00000448398.5:c.644A>C (ABCB6)
ENST00000494639.5:n.477A>C (ABCB6)
ENST00000497882.5:n.1881A>C (ABCB6)
NM_005689.2:c.1568A>C (ABCB6) NP_005680.1:p.Gln523Pro
NM_001349828.1:c.1430A>C (ABCB6) NP_001336757.1:p.Gln477Pro
NM_005689.3:c.1568A>C (ABCB6) NP_005680.1:p.Gln523Pro
NM_005689.4:c.1568A>C (ABCB6) MANE Select NP_005680.1:p.Gln523Pro
NM_001349828.2:c.1430A>C (ABCB6) NP_001336757.1:p.Gln477Pro