Canonical Allele Identifier: CA350681343

Gene: ABCB6 ATG9A

Linked Data

• MyVariant Identifiers: chr2:g.220074766T>G (hg19) ; chr2:g.219210044T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219210044T>G , CM000664.2:g.219210044T>G	GRCh38
NC_000002.11:g.220074766T>G , CM000664.1:g.220074766T>G	GRCh37
NC_000002.10:g.219783010T>G	NCBI36
NG_032110.1:g.13947A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265316.9:c.2423A>C (ABCB6) MANE Select	ENSP00000265316.3:p.His808Pro
ENST00000295750.5:c.2285A>C (ABCB6)	ENSP00000295750.5:p.His762Pro
ENST00000265316.7:c.2423A>C (ABCB6)	ENSP00000265316.3:p.His808Pro
ENST00000295750.4:c.1966A>C (ABCB6)
ENST00000443805.1:c.411A>C (ABCB6)
ENST00000446716.5:c.4973A>C (ATG9A)
ENST00000485773.5:n.690A>C (ABCB6)
ENST00000487380.5:n.496A>C (ABCB6)
ENST00000497882.5:n.2736A>C (ABCB6)
NM_005689.2:c.2423A>C (ABCB6)	NP_005680.1:p.His808Pro
NM_001349828.1:c.2285A>C (ABCB6)	NP_001336757.1:p.His762Pro
NM_005689.3:c.2423A>C (ABCB6)	NP_005680.1:p.His808Pro
NM_005689.4:c.2423A>C (ABCB6) MANE Select	NP_005680.1:p.His808Pro
NM_001349828.2:c.2285A>C (ABCB6)	NP_001336757.1:p.His762Pro