Canonical Allele Identifier: CA136880366

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs927613215
• gnomAD v4: 6-31657652-G-A
• MyVariant Identifiers: chr6:g.31625429G>A (hg19) ; chr6:g.31657652G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657652G>A , CM000668.2:g.31657652G>A	GRCh38
NC_000006.11:g.31625429G>A , CM000668.1:g.31625429G>A	GRCh37
NC_000006.10:g.31733408G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.470G>A (APOM) MANE Select	ENSP00000365081.3:p.Cys157Tyr
ENST00000375916.3:c.470G>A (APOM)	ENSP00000365081.3:p.Cys157Tyr
ENST00000375918.6:c.254G>A (APOM)	ENSP00000365083.2:p.Cys85Tyr
ENST00000375920.8:c.254G>A (APOM)	ENSP00000365085.4:p.Cys85Tyr
NM_001256169.1:c.254G>A (APOM)	NP_001243098.1:p.Cys85Tyr
NM_019101.2:c.470G>A (APOM)	NP_061974.2:p.Cys157Tyr
NR_045828.1:n.505G>A (APOM)
XM_006715150.2:c.374G>A (APOM)	XP_006715213.1:p.Cys125Tyr
XM_011514895.1:c.-14+2669C>T (BAG6)	XP_011513197.1:n.-14+2669C>T
XM_006715150.3:c.374G>A (APOM)	XP_006715213.1:p.Cys125Tyr
XM_017011279.2:c.-14+2669C>T (BAG6)	XP_016866768.1:n.-14+2669C>T
XM_024446545.1:c.-14+112C>T (BAG6)	XP_024302313.1:n.-14+112C>T
NM_019101.3:c.470G>A (APOM) MANE Select	NP_061974.2:p.Cys157Tyr
NM_001256169.2:c.254G>A (APOM)	NP_001243098.1:p.Cys85Tyr
NR_045828.2:n.511G>A (APOM)