Canonical Allele Identifier: CA1619250054

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1799980185

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655821G>C , CM000668.2:g.31655821G>C	GRCh38
NC_000006.11:g.31623598G>C , CM000668.1:g.31623598G>C	GRCh37
NC_000006.10:g.31731577G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.3:c.-146G>C (APOM)	ENSP00000365081.3:n.-146G>C
ENST00000375918.6:c.-102-651G>C (APOM)	ENSP00000365083.2:n.-102-651G>C
ENST00000375920.8:c.-102-651G>C (APOM)	ENSP00000365085.4:n.-102-651G>C
NM_001256169.1:c.-102-651G>C (APOM)	NP_001243098.1:n.-102-651G>C
NR_045828.1:n.143-651G>C (APOM)
XM_006715150.2:c.-249G>C (APOM)	XP_006715213.1:n.-249G>C
XM_011514895.1:c.-13-4045C>G (BAG6)	XP_011513197.1:n.-13-4045C>G
XM_017011279.2:c.-13-4045C>G (BAG6)	XP_016866768.1:n.-13-4045C>G
XM_024446545.1:c.-14+1943C>G (BAG6)	XP_024302313.1:n.-14+1943C>G
NM_001256169.2:c.-102-651G>C (APOM)	NP_001243098.1:n.-102-651G>C
NR_045828.2:n.149-651G>C (APOM)