Canonical Allele Identifier: CA136880302

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs900035633
• gnomAD v3: 6-31656762-G-A
• gnomAD v4: 6-31656762-G-A
• MyVariant Identifiers: chr6:g.31624539G>A (hg19) ; chr6:g.31656762G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656762G>A , CM000668.2:g.31656762G>A	GRCh38
NC_000006.11:g.31624539G>A , CM000668.1:g.31624539G>A	GRCh37
NC_000006.10:g.31732518G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.269+136G>A (APOM) MANE Select	ENSP00000365081.3:n.269+136G>A
ENST00000375916.3:c.269+136G>A (APOM)	ENSP00000365081.3:n.269+136G>A
ENST00000375918.6:c.53+136G>A (APOM)	ENSP00000365083.2:n.53+136G>A
ENST00000375920.8:c.53+136G>A (APOM)	ENSP00000365085.4:n.53+136G>A
NM_001256169.1:c.53+136G>A (APOM)	NP_001243098.1:n.53+136G>A
NM_019101.2:c.269+136G>A (APOM)	NP_061974.2:n.269+136G>A
NR_045828.1:n.304+129G>A (APOM)
XM_006715150.2:c.173+129G>A (APOM)	XP_006715213.1:n.173+129G>A
XM_011514895.1:c.-14+3559C>T (BAG6)	XP_011513197.1:n.-14+3559C>T
XM_006715150.3:c.173+129G>A (APOM)	XP_006715213.1:n.173+129G>A
XM_017011279.2:c.-14+3559C>T (BAG6)	XP_016866768.1:n.-14+3559C>T
XM_024446545.1:c.-14+1002C>T (BAG6)	XP_024302313.1:n.-14+1002C>T
NM_019101.3:c.269+136G>A (APOM) MANE Select	NP_061974.2:n.269+136G>A
NM_001256169.2:c.53+136G>A (APOM)	NP_001243098.1:n.53+136G>A
NR_045828.2:n.310+129G>A (APOM)