Canonical Allele Identifier: CA3718006

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs762203451
• ExAC: 6:31625218 T / C
• gnomAD v2: 6-31625218-T-C
• gnomAD v4: 6-31657441-T-C
• MyVariant Identifiers: chr6:g.31625218T>C (hg19) ; chr6:g.31657441T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657441T>C , CM000668.2:g.31657441T>C	GRCh38
NC_000006.11:g.31625218T>C , CM000668.1:g.31625218T>C	GRCh37
NC_000006.10:g.31733197T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.405T>C (APOM) MANE Select	ENSP00000365081.3:p.Asn135=
ENST00000375916.3:c.405T>C (APOM)	ENSP00000365081.3:p.Asn135=
ENST00000375918.6:c.189T>C (APOM)	ENSP00000365083.2:p.Asn63=
ENST00000375920.8:c.189T>C (APOM)	ENSP00000365085.4:p.Asn63=
NM_001256169.1:c.189T>C (APOM)	NP_001243098.1:p.Asn63=
NM_019101.2:c.405T>C (APOM)	NP_061974.2:p.Asn135=
NR_045828.1:n.440T>C (APOM)
XM_006715150.2:c.309T>C (APOM)	XP_006715213.1:p.Asn103=
XM_011514895.1:c.-14+2880A>G (BAG6)	XP_011513197.1:n.-14+2880A>G
XM_006715150.3:c.309T>C (APOM)	XP_006715213.1:p.Asn103=
XM_017011279.2:c.-14+2880A>G (BAG6)	XP_016866768.1:n.-14+2880A>G
XM_024446545.1:c.-14+323A>G (BAG6)	XP_024302313.1:n.-14+323A>G
NM_019101.3:c.405T>C (APOM) MANE Select	NP_061974.2:p.Asn135=
NM_001256169.2:c.189T>C (APOM)	NP_001243098.1:p.Asn63=
NR_045828.2:n.446T>C (APOM)