Canonical Allele Identifier: CA1329112420

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219213843T= , CM000664.2:g.219213843T= GRCh38
NC_000002.11:g.220078565T= , CM000664.1:g.220078565T= GRCh37
NC_000002.10:g.219786809T= NCBI36
NG_032110.1:g.10148A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.1561A= (ABCB6) MANE Select ENSP00000265316.3:p.Thr521=
ENST00000295750.5:c.1423A= (ABCB6) ENSP00000295750.5:p.Thr475=
ENST00000265316.7:c.1561A= (ABCB6) ENSP00000265316.3:p.Thr521=
ENST00000295750.4:c.1104A= (ABCB6)
ENST00000446716.5:c.4286A= (ATG9A)
ENST00000448398.5:c.637A= (ABCB6)
ENST00000494639.5:n.470A= (ABCB6)
ENST00000497882.5:n.1874A= (ABCB6)
NM_005689.2:c.1561A= (ABCB6) NP_005680.1:p.Thr521=
NM_001349828.1:c.1423A= (ABCB6) NP_001336757.1:p.Thr475=
NM_005689.3:c.1561A= (ABCB6) NP_005680.1:p.Thr521=
NM_005689.4:c.1561A= (ABCB6) MANE Select NP_005680.1:p.Thr521=
NM_001349828.2:c.1423A= (ABCB6) NP_001336757.1:p.Thr475=