Canonical Allele Identifier: CA363431184

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1341765956
• gnomAD v2: 6-31625528-G-A
• gnomAD v4: 6-31657751-G-A
• MyVariant Identifiers: chr6:g.31625528G>A (hg19) ; chr6:g.31657751G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657751G>A , CM000668.2:g.31657751G>A	GRCh38
NC_000006.11:g.31625528G>A , CM000668.1:g.31625528G>A	GRCh37
NC_000006.10:g.31733507G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.541+28G>A (APOM) MANE Select	ENSP00000365081.3:n.541+28G>A
ENST00000375916.3:c.541+28G>A (APOM)	ENSP00000365081.3:n.541+28G>A
ENST00000375918.6:c.353G>A (APOM)	ENSP00000365083.2:p.Gly118Glu
ENST00000375920.8:c.325+28G>A (APOM)	ENSP00000365085.4:n.325+28G>A
NM_001256169.1:c.325+28G>A (APOM)	NP_001243098.1:n.325+28G>A
NM_019101.2:c.541+28G>A (APOM)	NP_061974.2:n.541+28G>A
NR_045828.1:n.576+28G>A (APOM)
XM_006715150.2:c.445+28G>A (APOM)	XP_006715213.1:n.445+28G>A
XM_011514895.1:c.-14+2570C>T (BAG6)	XP_011513197.1:n.-14+2570C>T
XM_006715150.3:c.445+28G>A (APOM)	XP_006715213.1:n.445+28G>A
XM_017011279.2:c.-14+2570C>T (BAG6)	XP_016866768.1:n.-14+2570C>T
XM_024446545.1:c.-14+13C>T (BAG6)	XP_024302313.1:n.-14+13C>T
NM_019101.3:c.541+28G>A (APOM) MANE Select	NP_061974.2:n.541+28G>A
NM_001256169.2:c.325+28G>A (APOM)	NP_001243098.1:n.325+28G>A
NR_045828.2:n.582+28G>A (APOM)