Canonical Allele Identifier: CA363423486

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1209872725
• gnomAD v2: 6-31623775-A-G
• gnomAD v4: 6-31655998-A-G
• MyVariant Identifiers: chr6:g.31623775A>G (hg19) ; chr6:g.31655998A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655998A>G , CM000668.2:g.31655998A>G	GRCh38
NC_000006.11:g.31623775A>G , CM000668.1:g.31623775A>G	GRCh37
NC_000006.10:g.31731754A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.32A>G (APOM) MANE Select	ENSP00000365081.3:p.Tyr11Cys
ENST00000375916.3:c.32A>G (APOM)	ENSP00000365081.3:p.Tyr11Cys
ENST00000375918.6:c.-102-474A>G (APOM)	ENSP00000365083.2:n.-102-474A>G
ENST00000375920.8:c.-102-474A>G (APOM)	ENSP00000365085.4:n.-102-474A>G
NM_001256169.1:c.-102-474A>G (APOM)	NP_001243098.1:n.-102-474A>G
NM_019101.2:c.32A>G (APOM)	NP_061974.2:p.Tyr11Cys
NR_045828.1:n.143-474A>G (APOM)
XM_006715150.2:c.-72A>G (APOM)	XP_006715213.1:n.-72A>G
XM_011514895.1:c.-13-4222T>C (BAG6)	XP_011513197.1:n.-13-4222T>C
XM_006715150.3:c.-72A>G (APOM)	XP_006715213.1:n.-72A>G
XM_017011279.2:c.-13-4222T>C (BAG6)	XP_016866768.1:n.-13-4222T>C
XM_024446545.1:c.-14+1766T>C (BAG6)	XP_024302313.1:n.-14+1766T>C
NM_019101.3:c.32A>G (APOM) MANE Select	NP_061974.2:p.Tyr11Cys
NM_001256169.2:c.-102-474A>G (APOM)	NP_001243098.1:n.-102-474A>G
NR_045828.2:n.149-474A>G (APOM)