Canonical Allele Identifier: CA363423518

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs756613057
• MyVariant Identifiers: chr6:g.31623777T>A (hg19) ; chr6:g.31656000T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656000T>A , CM000668.2:g.31656000T>A	GRCh38
NC_000006.11:g.31623777T>A , CM000668.1:g.31623777T>A	GRCh37
NC_000006.10:g.31731756T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.34T>A (APOM) MANE Select	ENSP00000365081.3:p.Phe12Ile
ENST00000375916.3:c.34T>A (APOM)	ENSP00000365081.3:p.Phe12Ile
ENST00000375918.6:c.-102-472T>A (APOM)	ENSP00000365083.2:n.-102-472T>A
ENST00000375920.8:c.-102-472T>A (APOM)	ENSP00000365085.4:n.-102-472T>A
NM_001256169.1:c.-102-472T>A (APOM)	NP_001243098.1:n.-102-472T>A
NM_019101.2:c.34T>A (APOM)	NP_061974.2:p.Phe12Ile
NR_045828.1:n.143-472T>A (APOM)
XM_006715150.2:c.-70T>A (APOM)	XP_006715213.1:n.-70T>A
XM_011514895.1:c.-13-4224A>T (BAG6)	XP_011513197.1:n.-13-4224A>T
XM_006715150.3:c.-70T>A (APOM)	XP_006715213.1:n.-70T>A
XM_017011279.2:c.-13-4224A>T (BAG6)	XP_016866768.1:n.-13-4224A>T
XM_024446545.1:c.-14+1764A>T (BAG6)	XP_024302313.1:n.-14+1764A>T
NM_019101.3:c.34T>A (APOM) MANE Select	NP_061974.2:p.Phe12Ile
NM_001256169.2:c.-102-472T>A (APOM)	NP_001243098.1:n.-102-472T>A
NR_045828.2:n.149-472T>A (APOM)