Canonical Allele Identifier: CA350635078

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219213833T>C , CM000664.2:g.219213833T>C GRCh38
NC_000002.11:g.220078555T>C , CM000664.1:g.220078555T>C GRCh37
NC_000002.10:g.219786799T>C NCBI36
NG_032110.1:g.10158A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.1571A>G (ABCB6) MANE Select ENSP00000265316.3:p.Lys524Arg
ENST00000295750.5:c.1433A>G (ABCB6) ENSP00000295750.5:p.Lys478Arg
ENST00000265316.7:c.1571A>G (ABCB6) ENSP00000265316.3:p.Lys524Arg
ENST00000295750.4:c.1114A>G (ABCB6)
ENST00000446716.5:c.4296A>G (ATG9A)
ENST00000448398.5:c.647A>G (ABCB6)
ENST00000494639.5:n.480A>G (ABCB6)
ENST00000497882.5:n.1884A>G (ABCB6)
NM_005689.2:c.1571A>G (ABCB6) NP_005680.1:p.Lys524Arg
NM_001349828.1:c.1433A>G (ABCB6) NP_001336757.1:p.Lys478Arg
NM_005689.3:c.1571A>G (ABCB6) NP_005680.1:p.Lys524Arg
NM_005689.4:c.1571A>G (ABCB6) MANE Select NP_005680.1:p.Lys524Arg
NM_001349828.2:c.1433A>G (ABCB6) NP_001336757.1:p.Lys478Arg