Canonical Allele Identifier: CA350682777

Gene: ABCB6 ATG9A

Linked Data

• MyVariant Identifiers: chr2:g.220075449A>G (hg19) ; chr2:g.219210727A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219210727A>G , CM000664.2:g.219210727A>G	GRCh38
NC_000002.11:g.220075449A>G , CM000664.1:g.220075449A>G	GRCh37
NC_000002.10:g.219783693A>G	NCBI36
NG_032110.1:g.13264T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265316.9:c.2240T>C (ABCB6) MANE Select	ENSP00000265316.3:p.Ile747Thr
ENST00000295750.5:c.2102T>C (ABCB6)	ENSP00000295750.5:p.Ile701Thr
ENST00000265316.7:c.2240T>C (ABCB6)	ENSP00000265316.3:p.Ile747Thr
ENST00000295750.4:c.1783T>C (ABCB6)
ENST00000443805.1:c.228T>C (ABCB6)
ENST00000446716.5:c.4790T>C (ATG9A)
ENST00000485773.5:n.272T>C (ABCB6)
ENST00000487380.5:n.313T>C (ABCB6)
ENST00000492543.1:n.790T>C (ABCB6)
ENST00000497882.5:n.2553T>C (ABCB6)
NM_005689.2:c.2240T>C (ABCB6)	NP_005680.1:p.Ile747Thr
NM_001349828.1:c.2102T>C (ABCB6)	NP_001336757.1:p.Ile701Thr
NM_005689.3:c.2240T>C (ABCB6)	NP_005680.1:p.Ile747Thr
NM_005689.4:c.2240T>C (ABCB6) MANE Select	NP_005680.1:p.Ile747Thr
NM_001349828.2:c.2102T>C (ABCB6)	NP_001336757.1:p.Ile701Thr