Canonical Allele Identifier: CA363426772

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1355351268
• gnomAD v2: 6-31625004-A-C
• gnomAD v4: 6-31657227-A-C
• MyVariant Identifiers: chr6:g.31625004A>C (hg19) ; chr6:g.31657227A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657227A>C , CM000668.2:g.31657227A>C	GRCh38
NC_000006.11:g.31625004A>C , CM000668.1:g.31625004A>C	GRCh37
NC_000006.10:g.31732983A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.272A>C (APOM) MANE Select	ENSP00000365081.3:p.Lys91Thr
ENST00000375916.3:c.272A>C (APOM)	ENSP00000365081.3:p.Lys91Thr
ENST00000375918.6:c.56A>C (APOM)	ENSP00000365083.2:p.Lys19Thr
ENST00000375920.8:c.56A>C (APOM)	ENSP00000365085.4:p.Lys19Thr
NM_001256169.1:c.56A>C (APOM)	NP_001243098.1:p.Lys19Thr
NM_019101.2:c.272A>C (APOM)	NP_061974.2:p.Lys91Thr
NR_045828.1:n.307A>C (APOM)
XM_006715150.2:c.176A>C (APOM)	XP_006715213.1:p.Lys59Thr
XM_011514895.1:c.-14+3094T>G (BAG6)	XP_011513197.1:n.-14+3094T>G
XM_006715150.3:c.176A>C (APOM)	XP_006715213.1:p.Lys59Thr
XM_017011279.2:c.-14+3094T>G (BAG6)	XP_016866768.1:n.-14+3094T>G
XM_024446545.1:c.-14+537T>G (BAG6)	XP_024302313.1:n.-14+537T>G
NM_019101.3:c.272A>C (APOM) MANE Select	NP_061974.2:p.Lys91Thr
NM_001256169.2:c.56A>C (APOM)	NP_001243098.1:p.Lys19Thr
NR_045828.2:n.313A>C (APOM)