Canonical Allele Identifier: CA449667108

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625418T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657641T>G , CM000668.2:g.31657641T>G	GRCh38
NC_000006.11:g.31625418T>G , CM000668.1:g.31625418T>G	GRCh37
NC_000006.10:g.31733397T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.459T>G (APOM) MANE Select	ENSP00000365081.3:p.Pro153=
ENST00000375916.3:c.459T>G (APOM)	ENSP00000365081.3:p.Pro153=
ENST00000375918.6:c.243T>G (APOM)	ENSP00000365083.2:p.Pro81=
ENST00000375920.8:c.243T>G (APOM)	ENSP00000365085.4:p.Pro81=
NM_001256169.1:c.243T>G (APOM)	NP_001243098.1:p.Pro81=
NM_019101.2:c.459T>G (APOM)	NP_061974.2:p.Pro153=
NR_045828.1:n.494T>G (APOM)
XM_006715150.2:c.363T>G (APOM)	XP_006715213.1:p.Pro121=
XM_011514895.1:c.-14+2680A>C (BAG6)	XP_011513197.1:n.-14+2680A>C
XM_006715150.3:c.363T>G (APOM)	XP_006715213.1:p.Pro121=
XM_017011279.2:c.-14+2680A>C (BAG6)	XP_016866768.1:n.-14+2680A>C
XM_024446545.1:c.-14+123A>C (BAG6)	XP_024302313.1:n.-14+123A>C
NM_019101.3:c.459T>G (APOM) MANE Select	NP_061974.2:p.Pro153=
NM_001256169.2:c.243T>G (APOM)	NP_001243098.1:p.Pro81=
NR_045828.2:n.500T>G (APOM)