Canonical Allele Identifier: CA1619249362

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31654022G= , CM000668.2:g.31654022G=	GRCh38
NC_000006.11:g.31621799G= , CM000668.1:g.31621799G=	GRCh37
NC_000006.10:g.31729778G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375918.6:c.-103+1471G= (APOM)	ENSP00000365083.2:n.-103+1471G=
ENST00000375920.8:c.-103+1471G= (APOM)	ENSP00000365085.4:n.-103+1471G=
NM_001256169.1:c.-103+1471G= (APOM)	NP_001243098.1:n.-103+1471G=
NR_045828.1:n.142+1471G= (APOM)
XM_011514895.1:c.-13-2246C= (BAG6)	XP_011513197.1:n.-13-2246C=
XM_017011279.2:c.-13-2246C= (BAG6)	XP_016866768.1:n.-13-2246C=
XM_024446545.1:c.-13-2246C= (BAG6)	XP_024302313.1:n.-13-2246C=
NM_001256169.2:c.-103+1471G= (APOM)	NP_001243098.1:n.-103+1471G=
NR_045828.2:n.148+1471G= (APOM)