Canonical Allele Identifier: CA431422332

Gene: ABCB6 ATG9A

Linked Data

• MyVariant Identifiers: chr2:g.220075729T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219211007T>G , CM000664.2:g.219211007T>G	GRCh38
NC_000002.11:g.220075729T>G , CM000664.1:g.220075729T>G	GRCh37
NC_000002.10:g.219783973T>G	NCBI36
NG_032110.1:g.12984A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265316.9:c.2070A>C (ABCB6) MANE Select	ENSP00000265316.3:p.Thr690=
ENST00000295750.5:c.1932A>C (ABCB6)	ENSP00000295750.5:p.Thr644=
ENST00000265316.7:c.2070A>C (ABCB6)	ENSP00000265316.3:p.Thr690=
ENST00000295750.4:c.1613A>C (ABCB6)
ENST00000443805.1:c.32A>C (ABCB6)
ENST00000446716.5:c.4694-184A>C (ATG9A)
ENST00000485773.5:n.102A>C (ABCB6)
ENST00000487380.5:n.33A>C (ABCB6)
ENST00000492543.1:n.620A>C (ABCB6)
ENST00000497882.5:n.2383A>C (ABCB6)
NM_005689.2:c.2070A>C (ABCB6)	NP_005680.1:p.Thr690=
NM_001349828.1:c.1932A>C (ABCB6)	NP_001336757.1:p.Thr644=
NM_005689.3:c.2070A>C (ABCB6)	NP_005680.1:p.Thr690=
NM_005689.4:c.2070A>C (ABCB6) MANE Select	NP_005680.1:p.Thr690=
NM_001349828.2:c.1932A>C (ABCB6)	NP_001336757.1:p.Thr644=