Canonical Allele Identifier: CA3718035

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs750264591
• ExAC: 6:31625431 G / A
• gnomAD v2: 6-31625431-G-A
• gnomAD v4: 6-31657654-G-A
• COSMIC: COSM3861758 ; COSM3861759
• MyVariant Identifiers: chr6:g.31625431G>A (hg19) ; chr6:g.31657654G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657654G>A , CM000668.2:g.31657654G>A	GRCh38
NC_000006.11:g.31625431G>A , CM000668.1:g.31625431G>A	GRCh37
NC_000006.10:g.31733410G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.472G>A (APOM) MANE Select	ENSP00000365081.3:p.Val158Met
ENST00000375916.3:c.472G>A (APOM)	ENSP00000365081.3:p.Val158Met
ENST00000375918.6:c.256G>A (APOM)	ENSP00000365083.2:p.Val86Met
ENST00000375920.8:c.256G>A (APOM)	ENSP00000365085.4:p.Val86Met
NM_001256169.1:c.256G>A (APOM)	NP_001243098.1:p.Val86Met
NM_019101.2:c.472G>A (APOM)	NP_061974.2:p.Val158Met
NR_045828.1:n.507G>A (APOM)
XM_006715150.2:c.376G>A (APOM)	XP_006715213.1:p.Val126Met
XM_011514895.1:c.-14+2667C>T (BAG6)	XP_011513197.1:n.-14+2667C>T
XM_006715150.3:c.376G>A (APOM)	XP_006715213.1:p.Val126Met
XM_017011279.2:c.-14+2667C>T (BAG6)	XP_016866768.1:n.-14+2667C>T
XM_024446545.1:c.-14+110C>T (BAG6)	XP_024302313.1:n.-14+110C>T
NM_019101.3:c.472G>A (APOM) MANE Select	NP_061974.2:p.Val158Met
NM_001256169.2:c.256G>A (APOM)	NP_001243098.1:p.Val86Met
NR_045828.2:n.513G>A (APOM)