Canonical Allele Identifier: CA363423580

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31623780T>A (hg19) ; chr6:g.31656003T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656003T>A , CM000668.2:g.31656003T>A	GRCh38
NC_000006.11:g.31623780T>A , CM000668.1:g.31623780T>A	GRCh37
NC_000006.10:g.31731759T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.37T>A (APOM) MANE Select	ENSP00000365081.3:p.Tyr13Asn
ENST00000375916.3:c.37T>A (APOM)	ENSP00000365081.3:p.Tyr13Asn
ENST00000375918.6:c.-102-469T>A (APOM)	ENSP00000365083.2:n.-102-469T>A
ENST00000375920.8:c.-102-469T>A (APOM)	ENSP00000365085.4:n.-102-469T>A
NM_001256169.1:c.-102-469T>A (APOM)	NP_001243098.1:n.-102-469T>A
NM_019101.2:c.37T>A (APOM)	NP_061974.2:p.Tyr13Asn
NR_045828.1:n.143-469T>A (APOM)
XM_006715150.2:c.-67T>A (APOM)	XP_006715213.1:n.-67T>A
XM_011514895.1:c.-13-4227A>T (BAG6)	XP_011513197.1:n.-13-4227A>T
XM_006715150.3:c.-67T>A (APOM)	XP_006715213.1:n.-67T>A
XM_017011279.2:c.-13-4227A>T (BAG6)	XP_016866768.1:n.-13-4227A>T
XM_024446545.1:c.-14+1761A>T (BAG6)	XP_024302313.1:n.-14+1761A>T
NM_019101.3:c.37T>A (APOM) MANE Select	NP_061974.2:p.Tyr13Asn
NM_001256169.2:c.-102-469T>A (APOM)	NP_001243098.1:n.-102-469T>A
NR_045828.2:n.149-469T>A (APOM)