Canonical Allele Identifier: CA136880391

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs28432254
• gnomAD v4: 6-31658107-G-A
• MyVariant Identifiers: chr6:g.31625884G>A (hg19) ; chr6:g.31658107G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658107G>A , CM000668.2:g.31658107G>A	GRCh38
NC_000006.11:g.31625884G>A , CM000668.1:g.31625884G>A	GRCh37
NC_000006.10:g.31733863G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.*18G>A (APOM) MANE Select	ENSP00000365081.3:n.*18G>A
ENST00000375916.3:c.*18G>A (APOM)	ENSP00000365081.3:n.*18G>A
ENST00000375920.8:c.*18G>A (APOM)	ENSP00000365085.4:n.*18G>A
NM_001256169.1:c.*18G>A (APOM)	NP_001243098.1:n.*18G>A
NM_019101.2:c.*18G>A (APOM)	NP_061974.2:n.*18G>A
NR_045828.1:n.620G>A (APOM)
XM_006715150.2:c.*18G>A (APOM)	XP_006715213.1:n.*18G>A
XM_011514895.1:c.-14+2214C>T (BAG6)	XP_011513197.1:n.-14+2214C>T
XM_006715150.3:c.*18G>A (APOM)	XP_006715213.1:n.*18G>A
XM_017011279.2:c.-14+2214C>T (BAG6)	XP_016866768.1:n.-14+2214C>T
NM_019101.3:c.*18G>A (APOM) MANE Select	NP_061974.2:n.*18G>A
NM_001256169.2:c.*18G>A (APOM)	NP_001243098.1:n.*18G>A
NR_045828.2:n.626G>A (APOM)