Canonical Allele Identifier: CA566363734

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1156286505
• gnomAD v2: 6-31624608-A-G
• gnomAD v3: 6-31656831-A-G
• gnomAD v4: 6-31656831-A-G
• MyVariant Identifiers: chr6:g.31624608A>G (hg19) ; chr6:g.31656831A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656831A>G , CM000668.2:g.31656831A>G	GRCh38
NC_000006.11:g.31624608A>G , CM000668.1:g.31624608A>G	GRCh37
NC_000006.10:g.31732587A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.269+205A>G (APOM) MANE Select	ENSP00000365081.3:n.269+205A>G
ENST00000375916.3:c.269+205A>G (APOM)	ENSP00000365081.3:n.269+205A>G
ENST00000375918.6:c.53+205A>G (APOM)	ENSP00000365083.2:n.53+205A>G
ENST00000375920.8:c.53+205A>G (APOM)	ENSP00000365085.4:n.53+205A>G
NM_001256169.1:c.53+205A>G (APOM)	NP_001243098.1:n.53+205A>G
NM_019101.2:c.269+205A>G (APOM)	NP_061974.2:n.269+205A>G
NR_045828.1:n.304+198A>G (APOM)
XM_006715150.2:c.173+198A>G (APOM)	XP_006715213.1:n.173+198A>G
XM_011514895.1:c.-14+3490T>C (BAG6)	XP_011513197.1:n.-14+3490T>C
XM_006715150.3:c.173+198A>G (APOM)	XP_006715213.1:n.173+198A>G
XM_017011279.2:c.-14+3490T>C (BAG6)	XP_016866768.1:n.-14+3490T>C
XM_024446545.1:c.-14+933T>C (BAG6)	XP_024302313.1:n.-14+933T>C
NM_019101.3:c.269+205A>G (APOM) MANE Select	NP_061974.2:n.269+205A>G
NM_001256169.2:c.53+205A>G (APOM)	NP_001243098.1:n.53+205A>G
NR_045828.2:n.310+198A>G (APOM)