Canonical Allele Identifier: CA431421984

Gene: ABCB6 ATG9A

Linked Data

• MyVariant Identifiers: chr2:g.220075448G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219210726G>T , CM000664.2:g.219210726G>T	GRCh38
NC_000002.11:g.220075448G>T , CM000664.1:g.220075448G>T	GRCh37
NC_000002.10:g.219783692G>T	NCBI36
NG_032110.1:g.13265C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265316.9:c.2241C>A (ABCB6) MANE Select	ENSP00000265316.3:p.Ile747=
ENST00000295750.5:c.2103C>A (ABCB6)	ENSP00000295750.5:p.Ile701=
ENST00000265316.7:c.2241C>A (ABCB6)	ENSP00000265316.3:p.Ile747=
ENST00000295750.4:c.1784C>A (ABCB6)
ENST00000443805.1:c.229C>A (ABCB6)
ENST00000446716.5:c.4791C>A (ATG9A)
ENST00000485773.5:n.273C>A (ABCB6)
ENST00000487380.5:n.314C>A (ABCB6)
ENST00000492543.1:n.791C>A (ABCB6)
ENST00000497882.5:n.2554C>A (ABCB6)
NM_005689.2:c.2241C>A (ABCB6)	NP_005680.1:p.Ile747=
NM_001349828.1:c.2103C>A (ABCB6)	NP_001336757.1:p.Ile701=
NM_005689.3:c.2241C>A (ABCB6)	NP_005680.1:p.Ile747=
NM_005689.4:c.2241C>A (ABCB6) MANE Select	NP_005680.1:p.Ile747=
NM_001349828.2:c.2103C>A (ABCB6)	NP_001336757.1:p.Ile701=