Canonical Allele Identifier: CA363430018

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1432154791
• gnomAD v3: 6-31657625-A-T
• gnomAD v4: 6-31657625-A-T
• MyVariant Identifiers: chr6:g.31625402A>T (hg19) ; chr6:g.31657625A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657625A>T , CM000668.2:g.31657625A>T	GRCh38
NC_000006.11:g.31625402A>T , CM000668.1:g.31625402A>T	GRCh37
NC_000006.10:g.31733381A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.443A>T (APOM) MANE Select	ENSP00000365081.3:p.Asn148Ile
ENST00000375916.3:c.443A>T (APOM)	ENSP00000365081.3:p.Asn148Ile
ENST00000375918.6:c.227A>T (APOM)	ENSP00000365083.2:p.Asn76Ile
ENST00000375920.8:c.227A>T (APOM)	ENSP00000365085.4:p.Asn76Ile
NM_001256169.1:c.227A>T (APOM)	NP_001243098.1:p.Asn76Ile
NM_019101.2:c.443A>T (APOM)	NP_061974.2:p.Asn148Ile
NR_045828.1:n.478A>T (APOM)
XM_006715150.2:c.347A>T (APOM)	XP_006715213.1:p.Asn116Ile
XM_011514895.1:c.-14+2696T>A (BAG6)	XP_011513197.1:n.-14+2696T>A
XM_006715150.3:c.347A>T (APOM)	XP_006715213.1:p.Asn116Ile
XM_017011279.2:c.-14+2696T>A (BAG6)	XP_016866768.1:n.-14+2696T>A
XM_024446545.1:c.-14+139T>A (BAG6)	XP_024302313.1:n.-14+139T>A
NM_019101.3:c.443A>T (APOM) MANE Select	NP_061974.2:p.Asn148Ile
NM_001256169.2:c.227A>T (APOM)	NP_001243098.1:p.Asn76Ile
NR_045828.2:n.484A>T (APOM)