Canonical Allele Identifier: CA363431557

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1800334916
• gnomAD v4: 6-31658066-G-A
• MyVariant Identifiers: chr6:g.31625843G>A (hg19) ; chr6:g.31658066G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658066G>A , CM000668.2:g.31658066G>A	GRCh38
NC_000006.11:g.31625843G>A , CM000668.1:g.31625843G>A	GRCh37
NC_000006.10:g.31733822G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.544G>A (APOM) MANE Select	ENSP00000365081.3:p.Ala182Thr
ENST00000375916.3:c.544G>A (APOM)	ENSP00000365081.3:p.Ala182Thr
ENST00000375918.6:c.*278G>A (APOM)	ENSP00000365083.2:n.*278G>A
ENST00000375920.8:c.328G>A (APOM)	ENSP00000365085.4:p.Ala110Thr
NM_001256169.1:c.328G>A (APOM)	NP_001243098.1:p.Ala110Thr
NM_019101.2:c.544G>A (APOM)	NP_061974.2:p.Ala182Thr
NR_045828.1:n.579G>A (APOM)
XM_006715150.2:c.448G>A (APOM)	XP_006715213.1:p.Ala150Thr
XM_011514895.1:c.-14+2255C>T (BAG6)	XP_011513197.1:n.-14+2255C>T
XM_006715150.3:c.448G>A (APOM)	XP_006715213.1:p.Ala150Thr
XM_017011279.2:c.-14+2255C>T (BAG6)	XP_016866768.1:n.-14+2255C>T
NM_019101.3:c.544G>A (APOM) MANE Select	NP_061974.2:p.Ala182Thr
NM_001256169.2:c.328G>A (APOM)	NP_001243098.1:p.Ala110Thr
NR_045828.2:n.585G>A (APOM)