Canonical Allele Identifier: CA449667084

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1457170171
• gnomAD v2: 6-31625242-C-A
• gnomAD v3: 6-31657465-C-A
• gnomAD v4: 6-31657465-C-A
• MyVariant Identifiers: chr6:g.31625242C>A (hg19) ; chr6:g.31657465C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657465C>A , CM000668.2:g.31657465C>A	GRCh38
NC_000006.11:g.31625242C>A , CM000668.1:g.31625242C>A	GRCh37
NC_000006.10:g.31733221C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.429C>A (APOM) MANE Select	ENSP00000365081.3:p.Arg143=
ENST00000375916.3:c.429C>A (APOM)	ENSP00000365081.3:p.Arg143=
ENST00000375918.6:c.213C>A (APOM)	ENSP00000365083.2:p.Arg71=
ENST00000375920.8:c.213C>A (APOM)	ENSP00000365085.4:p.Arg71=
NM_001256169.1:c.213C>A (APOM)	NP_001243098.1:p.Arg71=
NM_019101.2:c.429C>A (APOM)	NP_061974.2:p.Arg143=
NR_045828.1:n.464C>A (APOM)
XM_006715150.2:c.333C>A (APOM)	XP_006715213.1:p.Arg111=
XM_011514895.1:c.-14+2856G>T (BAG6)	XP_011513197.1:n.-14+2856G>T
XM_006715150.3:c.333C>A (APOM)	XP_006715213.1:p.Arg111=
XM_017011279.2:c.-14+2856G>T (BAG6)	XP_016866768.1:n.-14+2856G>T
XM_024446545.1:c.-14+299G>T (BAG6)	XP_024302313.1:n.-14+299G>T
NM_019101.3:c.429C>A (APOM) MANE Select	NP_061974.2:p.Arg143=
NM_001256169.2:c.213C>A (APOM)	NP_001243098.1:p.Arg71=
NR_045828.2:n.470C>A (APOM)