Canonical Allele Identifier: CA823896524

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1420724178
• MyVariant Identifiers: chr6:g.31625778A>G (hg19) ; chr6:g.31658001A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658001A>G , CM000668.2:g.31658001A>G	GRCh38
NC_000006.11:g.31625778A>G , CM000668.1:g.31625778A>G	GRCh37
NC_000006.10:g.31733757A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.542-63A>G (APOM) MANE Select	ENSP00000365081.3:n.542-63A>G
ENST00000375916.3:c.542-63A>G (APOM)	ENSP00000365081.3:n.542-63A>G
ENST00000375918.6:c.*213A>G (APOM)	ENSP00000365083.2:n.*213A>G
ENST00000375920.8:c.326-63A>G (APOM)	ENSP00000365085.4:n.326-63A>G
NM_001256169.1:c.326-63A>G (APOM)	NP_001243098.1:n.326-63A>G
NM_019101.2:c.542-63A>G (APOM)	NP_061974.2:n.542-63A>G
NR_045828.1:n.577-63A>G (APOM)
XM_006715150.2:c.446-63A>G (APOM)	XP_006715213.1:n.446-63A>G
XM_011514895.1:c.-14+2320T>C (BAG6)	XP_011513197.1:n.-14+2320T>C
XM_006715150.3:c.446-63A>G (APOM)	XP_006715213.1:n.446-63A>G
XM_017011279.2:c.-14+2320T>C (BAG6)	XP_016866768.1:n.-14+2320T>C
NM_019101.3:c.542-63A>G (APOM) MANE Select	NP_061974.2:n.542-63A>G
NM_001256169.2:c.326-63A>G (APOM)	NP_001243098.1:n.326-63A>G
NR_045828.2:n.583-63A>G (APOM)