Canonical Allele Identifier: CA1329115464

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219218166T= , CM000664.2:g.219218166T= GRCh38
NC_000002.11:g.220082888T= , CM000664.1:g.220082888T= GRCh37
NC_000002.10:g.219791132T= NCBI36
NG_032110.1:g.5825A=

Transcript Alleles

HGVS Amino-acid Change
NM_005689.4:c.508A= (ABCB6) MANE Select NP_005680.1:p.Ser170=
ENST00000265316.9:c.508A= (ABCB6) MANE Select ENSP00000265316.3:p.Ser170=
NM_001349828.1:c.508A= (ABCB6) NP_001336757.1:p.Ser170=
NM_001349828.2:c.508A= (ABCB6) NP_001336757.1:p.Ser170=
NM_005689.2:c.508A= (ABCB6) NP_005680.1:p.Ser170=
NM_005689.3:c.508A= (ABCB6) NP_005680.1:p.Ser170=
ENST00000265316.7:c.508A= (ABCB6) ENSP00000265316.3:p.Ser170=
ENST00000295750.4:c.189A= (ABCB6)
ENST00000295750.5:c.508A= (ABCB6) ENSP00000295750.5:p.Ser170=
ENST00000417678.5:c.261A= (ABCB6)
ENST00000446716.5:c.3047A= (ATG9A)
ENST00000448398.5:c.311A= (ABCB6)
ENST00000452545.1:c.25A= (ABCB6) ENSP00000401811.1:p.Ser9=