Canonical Allele Identifier: CA449666511

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1309696253
• gnomAD v2: 6-31623806-C-T
• gnomAD v4: 6-31656029-C-T
• MyVariant Identifiers: chr6:g.31623806C>T (hg19) ; chr6:g.31656029C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656029C>T , CM000668.2:g.31656029C>T	GRCh38
NC_000006.11:g.31623806C>T , CM000668.1:g.31623806C>T	GRCh37
NC_000006.10:g.31731785C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.63C>T (APOM) MANE Select	ENSP00000365081.3:p.Tyr21=
ENST00000375916.3:c.63C>T (APOM)	ENSP00000365081.3:p.Tyr21=
ENST00000375918.6:c.-102-443C>T (APOM)	ENSP00000365083.2:n.-102-443C>T
ENST00000375920.8:c.-102-443C>T (APOM)	ENSP00000365085.4:n.-102-443C>T
NM_001256169.1:c.-102-443C>T (APOM)	NP_001243098.1:n.-102-443C>T
NM_019101.2:c.63C>T (APOM)	NP_061974.2:p.Tyr21=
NR_045828.1:n.143-443C>T (APOM)
XM_006715150.2:c.-41C>T (APOM)	XP_006715213.1:n.-41C>T
XM_011514895.1:c.-13-4253G>A (BAG6)	XP_011513197.1:n.-13-4253G>A
XM_006715150.3:c.-41C>T (APOM)	XP_006715213.1:n.-41C>T
XM_017011279.2:c.-13-4253G>A (BAG6)	XP_016866768.1:n.-13-4253G>A
XM_024446545.1:c.-14+1735G>A (BAG6)	XP_024302313.1:n.-14+1735G>A
NM_019101.3:c.63C>T (APOM) MANE Select	NP_061974.2:p.Tyr21=
NM_001256169.2:c.-102-443C>T (APOM)	NP_001243098.1:n.-102-443C>T
NR_045828.2:n.149-443C>T (APOM)