Canonical Allele Identifier: CA1619250988

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1800338938

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658118G>T , CM000668.2:g.31658118G>T	GRCh38
NC_000006.11:g.31625895G>T , CM000668.1:g.31625895G>T	GRCh37
NC_000006.10:g.31733874G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.*29G>T (APOM) MANE Select	ENSP00000365081.3:n.*29G>T
ENST00000375916.3:c.*29G>T (APOM)	ENSP00000365081.3:n.*29G>T
ENST00000375920.8:c.*29G>T (APOM)	ENSP00000365085.4:n.*29G>T
NM_001256169.1:c.*29G>T (APOM)	NP_001243098.1:n.*29G>T
NM_019101.2:c.*29G>T (APOM)	NP_061974.2:n.*29G>T
NR_045828.1:n.631G>T (APOM)
XM_006715150.2:c.*29G>T (APOM)	XP_006715213.1:n.*29G>T
XM_011514895.1:c.-14+2203C>A (BAG6)	XP_011513197.1:n.-14+2203C>A
XM_006715150.3:c.*29G>T (APOM)	XP_006715213.1:n.*29G>T
XM_017011279.2:c.-14+2203C>A (BAG6)	XP_016866768.1:n.-14+2203C>A
NM_019101.3:c.*29G>T (APOM) MANE Select	NP_061974.2:n.*29G>T
NM_001256169.2:c.*29G>T (APOM)	NP_001243098.1:n.*29G>T
NR_045828.2:n.637G>T (APOM)