Canonical Allele Identifier: CA566364080

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1228942414
• gnomAD v2: 6-31625132-A-G
• gnomAD v3: 6-31657355-A-G
• gnomAD v4: 6-31657355-A-G
• MyVariant Identifiers: chr6:g.31625132A>G (hg19) ; chr6:g.31657355A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657355A>G , CM000668.2:g.31657355A>G	GRCh38
NC_000006.11:g.31625132A>G , CM000668.1:g.31625132A>G	GRCh37
NC_000006.10:g.31733111A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.344-25A>G (APOM) MANE Select	ENSP00000365081.3:n.344-25A>G
ENST00000375916.3:c.344-25A>G (APOM)	ENSP00000365081.3:n.344-25A>G
ENST00000375918.6:c.128-25A>G (APOM)	ENSP00000365083.2:n.128-25A>G
ENST00000375920.8:c.128-25A>G (APOM)	ENSP00000365085.4:n.128-25A>G
NM_001256169.1:c.128-25A>G (APOM)	NP_001243098.1:n.128-25A>G
NM_019101.2:c.344-25A>G (APOM)	NP_061974.2:n.344-25A>G
NR_045828.1:n.379-25A>G (APOM)
XM_006715150.2:c.248-25A>G (APOM)	XP_006715213.1:n.248-25A>G
XM_011514895.1:c.-14+2966T>C (BAG6)	XP_011513197.1:n.-14+2966T>C
XM_006715150.3:c.248-25A>G (APOM)	XP_006715213.1:n.248-25A>G
XM_017011279.2:c.-14+2966T>C (BAG6)	XP_016866768.1:n.-14+2966T>C
XM_024446545.1:c.-14+409T>C (BAG6)	XP_024302313.1:n.-14+409T>C
NM_019101.3:c.344-25A>G (APOM) MANE Select	NP_061974.2:n.344-25A>G
NM_001256169.2:c.128-25A>G (APOM)	NP_001243098.1:n.128-25A>G
NR_045828.2:n.385-25A>G (APOM)