Canonical Allele Identifier: CA566690928

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs372408015
• gnomAD v2: 6-31625281-G-C
• gnomAD v4: 6-31657504-G-C
• MyVariant Identifiers: chr6:g.31625281G>C (hg19) ; chr6:g.31657504G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657504G>C , CM000668.2:g.31657504G>C	GRCh38
NC_000006.11:g.31625281G>C , CM000668.1:g.31625281G>C	GRCh37
NC_000006.10:g.31733260G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.442+26G>C (APOM) MANE Select	ENSP00000365081.3:n.442+26G>C
ENST00000375916.3:c.442+26G>C (APOM)	ENSP00000365081.3:n.442+26G>C
ENST00000375918.6:c.226+26G>C (APOM)	ENSP00000365083.2:n.226+26G>C
ENST00000375920.8:c.226+26G>C (APOM)	ENSP00000365085.4:n.226+26G>C
NM_001256169.1:c.226+26G>C (APOM)	NP_001243098.1:n.226+26G>C
NM_019101.2:c.442+26G>C (APOM)	NP_061974.2:n.442+26G>C
NR_045828.1:n.477+26G>C (APOM)
XM_006715150.2:c.346+26G>C (APOM)	XP_006715213.1:n.346+26G>C
XM_011514895.1:c.-14+2817C>G (BAG6)	XP_011513197.1:n.-14+2817C>G
XM_006715150.3:c.346+26G>C (APOM)	XP_006715213.1:n.346+26G>C
XM_017011279.2:c.-14+2817C>G (BAG6)	XP_016866768.1:n.-14+2817C>G
XM_024446545.1:c.-14+260C>G (BAG6)	XP_024302313.1:n.-14+260C>G
NM_019101.3:c.442+26G>C (APOM) MANE Select	NP_061974.2:n.442+26G>C
NM_001256169.2:c.226+26G>C (APOM)	NP_001243098.1:n.226+26G>C
NR_045828.2:n.483+26G>C (APOM)