Canonical Allele Identifier: CA823904367

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1379343298
• gnomAD v3: 6-31655690-AG-A
• gnomAD v4: 6-31655690-AG-A
• MyVariant Identifiers: chr6:g.31623468del (hg19) ; chr6:g.31655691del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655692del , CM000668.2:g.31655692del	GRCh38
NC_000006.11:g.31623469del , CM000668.1:g.31623469del	GRCh37
NC_000006.10:g.31731448del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.3:c.-275del (APOM)	ENSP00000365081.3:n.-275del
ENST00000375918.6:c.-102-780del (APOM)	ENSP00000365083.2:n.-102-780del
ENST00000375920.8:c.-102-780del (APOM)	ENSP00000365085.4:n.-102-780del
NM_001256169.1:c.-102-780del (APOM)	NP_001243098.1:n.-102-780del
NR_045828.1:n.143-780del (APOM)
XM_006715150.2:c.-378del (APOM)	XP_006715213.1:n.-378del
XM_011514895.1:c.-13-3915del (BAG6)	XP_011513197.1:n.-13-3915del
XM_017011279.2:c.-13-3915del (BAG6)	XP_016866768.1:n.-13-3915del
XM_024446545.1:c.-14+2073del (BAG6)	XP_024302313.1:n.-14+2073del
NM_001256169.2:c.-102-780del (APOM)	NP_001243098.1:n.-102-780del
NR_045828.2:n.149-780del (APOM)