Canonical Allele Identifier: CA136880367

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs770349792
• gnomAD v4: 6-31657694-A-C
• MyVariant Identifiers: chr6:g.31625471A>C (hg19) ; chr6:g.31657694A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657694A>C , CM000668.2:g.31657694A>C	GRCh38
NC_000006.11:g.31625471A>C , CM000668.1:g.31625471A>C	GRCh37
NC_000006.10:g.31733450A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.512A>C (APOM) MANE Select	ENSP00000365081.3:p.Lys171Thr
ENST00000375916.3:c.512A>C (APOM)	ENSP00000365081.3:p.Lys171Thr
ENST00000375918.6:c.296A>C (APOM)	ENSP00000365083.2:p.Lys99Thr
ENST00000375920.8:c.296A>C (APOM)	ENSP00000365085.4:p.Lys99Thr
NM_001256169.1:c.296A>C (APOM)	NP_001243098.1:p.Lys99Thr
NM_019101.2:c.512A>C (APOM)	NP_061974.2:p.Lys171Thr
NR_045828.1:n.547A>C (APOM)
XM_006715150.2:c.416A>C (APOM)	XP_006715213.1:p.Lys139Thr
XM_011514895.1:c.-14+2627T>G (BAG6)	XP_011513197.1:n.-14+2627T>G
XM_006715150.3:c.416A>C (APOM)	XP_006715213.1:p.Lys139Thr
XM_017011279.2:c.-14+2627T>G (BAG6)	XP_016866768.1:n.-14+2627T>G
XM_024446545.1:c.-14+70T>G (BAG6)	XP_024302313.1:n.-14+70T>G
NM_019101.3:c.512A>C (APOM) MANE Select	NP_061974.2:p.Lys171Thr
NM_001256169.2:c.296A>C (APOM)	NP_001243098.1:p.Lys99Thr
NR_045828.2:n.553A>C (APOM)