Canonical Allele Identifier: CA136880356

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1015492900
• gnomAD v2: 6-31625228-C-T
• gnomAD v3: 6-31657451-C-T
• gnomAD v4: 6-31657451-C-T
• MyVariant Identifiers: chr6:g.31625228C>T (hg19) ; chr6:g.31657451C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657451C>T , CM000668.2:g.31657451C>T	GRCh38
NC_000006.11:g.31625228C>T , CM000668.1:g.31625228C>T	GRCh37
NC_000006.10:g.31733207C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.415C>T (APOM) MANE Select	ENSP00000365081.3:p.Gln139Ter
ENST00000375916.3:c.415C>T (APOM)	ENSP00000365081.3:p.Gln139Ter
ENST00000375918.6:c.199C>T (APOM)	ENSP00000365083.2:p.Gln67Ter
ENST00000375920.8:c.199C>T (APOM)	ENSP00000365085.4:p.Gln67Ter
NM_001256169.1:c.199C>T (APOM)	NP_001243098.1:p.Gln67Ter
NM_019101.2:c.415C>T (APOM)	NP_061974.2:p.Gln139Ter
NR_045828.1:n.450C>T (APOM)
XM_006715150.2:c.319C>T (APOM)	XP_006715213.1:p.Gln107Ter
XM_011514895.1:c.-14+2870G>A (BAG6)	XP_011513197.1:n.-14+2870G>A
XM_006715150.3:c.319C>T (APOM)	XP_006715213.1:p.Gln107Ter
XM_017011279.2:c.-14+2870G>A (BAG6)	XP_016866768.1:n.-14+2870G>A
XM_024446545.1:c.-14+313G>A (BAG6)	XP_024302313.1:n.-14+313G>A
NM_019101.3:c.415C>T (APOM) MANE Select	NP_061974.2:p.Gln139Ter
NM_001256169.2:c.199C>T (APOM)	NP_001243098.1:p.Gln67Ter
NR_045828.2:n.456C>T (APOM)