Canonical Allele Identifier: CA449667210

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625857C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658080C>G , CM000668.2:g.31658080C>G	GRCh38
NC_000006.11:g.31625857C>G , CM000668.1:g.31625857C>G	GRCh37
NC_000006.10:g.31733836C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.558C>G (APOM) MANE Select	ENSP00000365081.3:p.Ser186=
ENST00000375916.3:c.558C>G (APOM)	ENSP00000365081.3:p.Ser186=
ENST00000375918.6:c.*292C>G (APOM)	ENSP00000365083.2:n.*292C>G
ENST00000375920.8:c.342C>G (APOM)	ENSP00000365085.4:p.Ser114=
NM_001256169.1:c.342C>G (APOM)	NP_001243098.1:p.Ser114=
NM_019101.2:c.558C>G (APOM)	NP_061974.2:p.Ser186=
NR_045828.1:n.593C>G (APOM)
XM_006715150.2:c.462C>G (APOM)	XP_006715213.1:p.Ser154=
XM_011514895.1:c.-14+2241G>C (BAG6)	XP_011513197.1:n.-14+2241G>C
XM_006715150.3:c.462C>G (APOM)	XP_006715213.1:p.Ser154=
XM_017011279.2:c.-14+2241G>C (BAG6)	XP_016866768.1:n.-14+2241G>C
NM_019101.3:c.558C>G (APOM) MANE Select	NP_061974.2:p.Ser186=
NM_001256169.2:c.342C>G (APOM)	NP_001243098.1:p.Ser114=
NR_045828.2:n.599C>G (APOM)