Canonical Allele Identifier: CA1087476611

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1799962932
• gnomAD v3: 6-31655694-T-G
• gnomAD v4: 6-31655694-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655694T>G , CM000668.2:g.31655694T>G	GRCh38
NC_000006.11:g.31623471T>G , CM000668.1:g.31623471T>G	GRCh37
NC_000006.10:g.31731450T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.3:c.-273T>G (APOM)	ENSP00000365081.3:n.-273T>G
ENST00000375918.6:c.-102-778T>G (APOM)	ENSP00000365083.2:n.-102-778T>G
ENST00000375920.8:c.-102-778T>G (APOM)	ENSP00000365085.4:n.-102-778T>G
NM_001256169.1:c.-102-778T>G (APOM)	NP_001243098.1:n.-102-778T>G
NR_045828.1:n.143-778T>G (APOM)
XM_006715150.2:c.-376T>G (APOM)	XP_006715213.1:n.-376T>G
XM_011514895.1:c.-13-3918A>C (BAG6)	XP_011513197.1:n.-13-3918A>C
XM_017011279.2:c.-13-3918A>C (BAG6)	XP_016866768.1:n.-13-3918A>C
XM_024446545.1:c.-14+2070A>C (BAG6)	XP_024302313.1:n.-14+2070A>C
NM_001256169.2:c.-102-778T>G (APOM)	NP_001243098.1:n.-102-778T>G
NR_045828.2:n.149-778T>G (APOM)