Canonical Allele Identifier: CA2677983881

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657584-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657584C>T , CM000668.2:g.31657584C>T	GRCh38
NC_000006.11:g.31625361C>T , CM000668.1:g.31625361C>T	GRCh37
NC_000006.10:g.31733340C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.443-41C>T (APOM) MANE Select	ENSP00000365081.3:n.443-41C>T
ENST00000375916.3:c.443-41C>T (APOM)	ENSP00000365081.3:n.443-41C>T
ENST00000375918.6:c.227-41C>T (APOM)	ENSP00000365083.2:n.227-41C>T
ENST00000375920.8:c.227-41C>T (APOM)	ENSP00000365085.4:n.227-41C>T
NM_001256169.1:c.227-41C>T (APOM)	NP_001243098.1:n.227-41C>T
NM_019101.2:c.443-41C>T (APOM)	NP_061974.2:n.443-41C>T
NR_045828.1:n.478-41C>T (APOM)
XM_006715150.2:c.347-41C>T (APOM)	XP_006715213.1:n.347-41C>T
XM_011514895.1:c.-14+2737G>A (BAG6)	XP_011513197.1:n.-14+2737G>A
XM_006715150.3:c.347-41C>T (APOM)	XP_006715213.1:n.347-41C>T
XM_017011279.2:c.-14+2737G>A (BAG6)	XP_016866768.1:n.-14+2737G>A
XM_024446545.1:c.-14+180G>A (BAG6)	XP_024302313.1:n.-14+180G>A
NM_019101.3:c.443-41C>T (APOM) MANE Select	NP_061974.2:n.443-41C>T
NM_001256169.2:c.227-41C>T (APOM)	NP_001243098.1:n.227-41C>T
NR_045828.2:n.484-41C>T (APOM)