Canonical Allele Identifier: CA823896713

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1160126705
• gnomAD v4: 6-31658166-C-G
• MyVariant Identifiers: chr6:g.31625943C>G (hg19) ; chr6:g.31658166C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658166C>G , CM000668.2:g.31658166C>G	GRCh38
NC_000006.11:g.31625943C>G , CM000668.1:g.31625943C>G	GRCh37
NC_000006.10:g.31733922C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.*77C>G (APOM) MANE Select	ENSP00000365081.3:n.*77C>G
ENST00000375916.3:c.*77C>G (APOM)	ENSP00000365081.3:n.*77C>G
ENST00000375920.8:c.*77C>G (APOM)	ENSP00000365085.4:n.*77C>G
NM_001256169.1:c.*77C>G (APOM)	NP_001243098.1:n.*77C>G
NM_019101.2:c.*77C>G (APOM)	NP_061974.2:n.*77C>G
NR_045828.1:n.679C>G (APOM)
XM_006715150.2:c.*77C>G (APOM)	XP_006715213.1:n.*77C>G
XM_011514895.1:c.-14+2155G>C (BAG6)	XP_011513197.1:n.-14+2155G>C
XM_006715150.3:c.*77C>G (APOM)	XP_006715213.1:n.*77C>G
XM_017011279.2:c.-14+2155G>C (BAG6)	XP_016866768.1:n.-14+2155G>C
NM_019101.3:c.*77C>G (APOM) MANE Select	NP_061974.2:n.*77C>G
NM_001256169.2:c.*77C>G (APOM)	NP_001243098.1:n.*77C>G
NR_045828.2:n.685C>G (APOM)