Canonical Allele Identifier: CA449666481

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1212243104
• gnomAD v4: 6-31656005-T-C
• MyVariant Identifiers: chr6:g.31623782T>C (hg19) ; chr6:g.31656005T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656005T>C , CM000668.2:g.31656005T>C	GRCh38
NC_000006.11:g.31623782T>C , CM000668.1:g.31623782T>C	GRCh37
NC_000006.10:g.31731761T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.39T>C (APOM) MANE Select	ENSP00000365081.3:p.Tyr13=
ENST00000375916.3:c.39T>C (APOM)	ENSP00000365081.3:p.Tyr13=
ENST00000375918.6:c.-102-467T>C (APOM)	ENSP00000365083.2:n.-102-467T>C
ENST00000375920.8:c.-102-467T>C (APOM)	ENSP00000365085.4:n.-102-467T>C
NM_001256169.1:c.-102-467T>C (APOM)	NP_001243098.1:n.-102-467T>C
NM_019101.2:c.39T>C (APOM)	NP_061974.2:p.Tyr13=
NR_045828.1:n.143-467T>C (APOM)
XM_006715150.2:c.-65T>C (APOM)	XP_006715213.1:n.-65T>C
XM_011514895.1:c.-13-4229A>G (BAG6)	XP_011513197.1:n.-13-4229A>G
XM_006715150.3:c.-65T>C (APOM)	XP_006715213.1:n.-65T>C
XM_017011279.2:c.-13-4229A>G (BAG6)	XP_016866768.1:n.-13-4229A>G
XM_024446545.1:c.-14+1759A>G (BAG6)	XP_024302313.1:n.-14+1759A>G
NM_019101.3:c.39T>C (APOM) MANE Select	NP_061974.2:p.Tyr13=
NM_001256169.2:c.-102-467T>C (APOM)	NP_001243098.1:n.-102-467T>C
NR_045828.2:n.149-467T>C (APOM)