Canonical Allele Identifier: CA2663211910

Gene: ABCB6 ATG9A

Linked Data

• gnomAD v4: 2-219210655-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219210655A>G , CM000664.2:g.219210655A>G	GRCh38
NC_000002.11:g.220075377A>G , CM000664.1:g.220075377A>G	GRCh37
NC_000002.10:g.219783621A>G	NCBI36
NG_032110.1:g.13336T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265316.9:c.2256+56T>C (ABCB6) MANE Select	ENSP00000265316.3:n.2256+56T>C
ENST00000295750.5:c.2118+56T>C (ABCB6)	ENSP00000295750.5:n.2118+56T>C
ENST00000265316.7:c.2256+56T>C (ABCB6)	ENSP00000265316.3:n.2256+56T>C
ENST00000295750.4:c.1799+56T>C (ABCB6)
ENST00000443805.1:c.244+56T>C (ABCB6)
ENST00000446716.5:c.4806+56T>C (ATG9A)
ENST00000485773.5:n.344T>C (ABCB6)
ENST00000487380.5:n.329+56T>C (ABCB6)
ENST00000497882.5:n.2569+56T>C (ABCB6)
NM_005689.2:c.2256+56T>C (ABCB6)	NP_005680.1:n.2256+56T>C
NM_001349828.1:c.2118+56T>C (ABCB6)	NP_001336757.1:n.2118+56T>C
NM_005689.3:c.2256+56T>C (ABCB6)	NP_005680.1:n.2256+56T>C
NM_005689.4:c.2256+56T>C (ABCB6) MANE Select	NP_005680.1:n.2256+56T>C
NM_001349828.2:c.2118+56T>C (ABCB6)	NP_001336757.1:n.2118+56T>C