Canonical Allele Identifier: CA363423928

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31623805A>C (hg19) ; chr6:g.31656028A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656028A>C , CM000668.2:g.31656028A>C	GRCh38
NC_000006.11:g.31623805A>C , CM000668.1:g.31623805A>C	GRCh37
NC_000006.10:g.31731784A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.62A>C (APOM) MANE Select	ENSP00000365081.3:p.Tyr21Ser
ENST00000375916.3:c.62A>C (APOM)	ENSP00000365081.3:p.Tyr21Ser
ENST00000375918.6:c.-102-444A>C (APOM)	ENSP00000365083.2:n.-102-444A>C
ENST00000375920.8:c.-102-444A>C (APOM)	ENSP00000365085.4:n.-102-444A>C
NM_001256169.1:c.-102-444A>C (APOM)	NP_001243098.1:n.-102-444A>C
NM_019101.2:c.62A>C (APOM)	NP_061974.2:p.Tyr21Ser
NR_045828.1:n.143-444A>C (APOM)
XM_006715150.2:c.-42A>C (APOM)	XP_006715213.1:n.-42A>C
XM_011514895.1:c.-13-4252T>G (BAG6)	XP_011513197.1:n.-13-4252T>G
XM_006715150.3:c.-42A>C (APOM)	XP_006715213.1:n.-42A>C
XM_017011279.2:c.-13-4252T>G (BAG6)	XP_016866768.1:n.-13-4252T>G
XM_024446545.1:c.-14+1736T>G (BAG6)	XP_024302313.1:n.-14+1736T>G
NM_019101.3:c.62A>C (APOM) MANE Select	NP_061974.2:p.Tyr21Ser
NM_001256169.2:c.-102-444A>C (APOM)	NP_001243098.1:n.-102-444A>C
NR_045828.2:n.149-444A>C (APOM)