Canonical Allele Identifier: CA449667087

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625245T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657468T>C , CM000668.2:g.31657468T>C	GRCh38
NC_000006.11:g.31625245T>C , CM000668.1:g.31625245T>C	GRCh37
NC_000006.10:g.31733224T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.432T>C (APOM) MANE Select	ENSP00000365081.3:p.Phe144=
ENST00000375916.3:c.432T>C (APOM)	ENSP00000365081.3:p.Phe144=
ENST00000375918.6:c.216T>C (APOM)	ENSP00000365083.2:p.Phe72=
ENST00000375920.8:c.216T>C (APOM)	ENSP00000365085.4:p.Phe72=
NM_001256169.1:c.216T>C (APOM)	NP_001243098.1:p.Phe72=
NM_019101.2:c.432T>C (APOM)	NP_061974.2:p.Phe144=
NR_045828.1:n.467T>C (APOM)
XM_006715150.2:c.336T>C (APOM)	XP_006715213.1:p.Phe112=
XM_011514895.1:c.-14+2853A>G (BAG6)	XP_011513197.1:n.-14+2853A>G
XM_006715150.3:c.336T>C (APOM)	XP_006715213.1:p.Phe112=
XM_017011279.2:c.-14+2853A>G (BAG6)	XP_016866768.1:n.-14+2853A>G
XM_024446545.1:c.-14+296A>G (BAG6)	XP_024302313.1:n.-14+296A>G
NM_019101.3:c.432T>C (APOM) MANE Select	NP_061974.2:p.Phe144=
NM_001256169.2:c.216T>C (APOM)	NP_001243098.1:p.Phe72=
NR_045828.2:n.473T>C (APOM)