Canonical Allele Identifier: CA1619251006

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1800345635

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658161T>G , CM000668.2:g.31658161T>G	GRCh38
NC_000006.11:g.31625938T>G , CM000668.1:g.31625938T>G	GRCh37
NC_000006.10:g.31733917T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.*72T>G (APOM) MANE Select	ENSP00000365081.3:n.*72T>G
ENST00000375916.3:c.*72T>G (APOM)	ENSP00000365081.3:n.*72T>G
ENST00000375920.8:c.*72T>G (APOM)	ENSP00000365085.4:n.*72T>G
NM_001256169.1:c.*72T>G (APOM)	NP_001243098.1:n.*72T>G
NM_019101.2:c.*72T>G (APOM)	NP_061974.2:n.*72T>G
NR_045828.1:n.674T>G (APOM)
XM_006715150.2:c.*72T>G (APOM)	XP_006715213.1:n.*72T>G
XM_011514895.1:c.-14+2160A>C (BAG6)	XP_011513197.1:n.-14+2160A>C
XM_006715150.3:c.*72T>G (APOM)	XP_006715213.1:n.*72T>G
XM_017011279.2:c.-14+2160A>C (BAG6)	XP_016866768.1:n.-14+2160A>C
NM_019101.3:c.*72T>G (APOM) MANE Select	NP_061974.2:n.*72T>G
NM_001256169.2:c.*72T>G (APOM)	NP_001243098.1:n.*72T>G
NR_045828.2:n.680T>G (APOM)