Canonical Allele Identifier: CA363431742

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625861A>G (hg19) ; chr6:g.31658084A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658084A>G , CM000668.2:g.31658084A>G	GRCh38
NC_000006.11:g.31625861A>G , CM000668.1:g.31625861A>G	GRCh37
NC_000006.10:g.31733840A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.562A>G (APOM) MANE Select	ENSP00000365081.3:p.Asn188Asp
ENST00000375916.3:c.562A>G (APOM)	ENSP00000365081.3:p.Asn188Asp
ENST00000375920.8:c.346A>G (APOM)	ENSP00000365085.4:p.Asn116Asp
NM_001256169.1:c.346A>G (APOM)	NP_001243098.1:p.Asn116Asp
NM_019101.2:c.562A>G (APOM)	NP_061974.2:p.Asn188Asp
NR_045828.1:n.597A>G (APOM)
XM_006715150.2:c.466A>G (APOM)	XP_006715213.1:p.Asn156Asp
XM_011514895.1:c.-14+2237T>C (BAG6)	XP_011513197.1:n.-14+2237T>C
XM_006715150.3:c.466A>G (APOM)	XP_006715213.1:p.Asn156Asp
XM_017011279.2:c.-14+2237T>C (BAG6)	XP_016866768.1:n.-14+2237T>C
NM_019101.3:c.562A>G (APOM) MANE Select	NP_061974.2:p.Asn188Asp
NM_001256169.2:c.346A>G (APOM)	NP_001243098.1:p.Asn116Asp
NR_045828.2:n.603A>G (APOM)