Canonical Allele Identifier: CA1329112321

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219213766C= , CM000664.2:g.219213766C= GRCh38
NC_000002.11:g.220078488C= , CM000664.1:g.220078488C= GRCh37
NC_000002.10:g.219786732C= NCBI36
NG_032110.1:g.10225G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.1578+60G= (ABCB6) MANE Select ENSP00000265316.3:n.1578+60G=
ENST00000295750.5:c.1440+60G= (ABCB6) ENSP00000295750.5:n.1440+60G=
ENST00000265316.7:c.1578+60G= (ABCB6) ENSP00000265316.3:n.1578+60G=
ENST00000295750.4:c.1121+60G= (ABCB6)
ENST00000446716.5:c.4303+60G= (ATG9A)
ENST00000448398.5:c.654+60G= (ABCB6)
ENST00000494639.5:n.487+60G= (ABCB6)
ENST00000497882.5:n.1891+60G= (ABCB6)
NM_005689.2:c.1578+60G= (ABCB6) NP_005680.1:n.1578+60G=
NM_001349828.1:c.1440+60G= (ABCB6) NP_001336757.1:n.1440+60G=
NM_005689.3:c.1578+60G= (ABCB6) NP_005680.1:n.1578+60G=
NM_005689.4:c.1578+60G= (ABCB6) MANE Select NP_005680.1:n.1578+60G=
NM_001349828.2:c.1440+60G= (ABCB6) NP_001336757.1:n.1440+60G=