Canonical Allele Identifier: CA449666474

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs766981599
• gnomAD v3: 6-31655996-C-T
• gnomAD v4: 6-31655996-C-T
• MyVariant Identifiers: chr6:g.31623773C>T (hg19) ; chr6:g.31655996C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655996C>T , CM000668.2:g.31655996C>T	GRCh38
NC_000006.11:g.31623773C>T , CM000668.1:g.31623773C>T	GRCh37
NC_000006.10:g.31731752C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.30C>T (APOM) MANE Select	ENSP00000365081.3:p.Leu10=
ENST00000375916.3:c.30C>T (APOM)	ENSP00000365081.3:p.Leu10=
ENST00000375918.6:c.-102-476C>T (APOM)	ENSP00000365083.2:n.-102-476C>T
ENST00000375920.8:c.-102-476C>T (APOM)	ENSP00000365085.4:n.-102-476C>T
NM_001256169.1:c.-102-476C>T (APOM)	NP_001243098.1:n.-102-476C>T
NM_019101.2:c.30C>T (APOM)	NP_061974.2:p.Leu10=
NR_045828.1:n.143-476C>T (APOM)
XM_006715150.2:c.-74C>T (APOM)	XP_006715213.1:n.-74C>T
XM_011514895.1:c.-13-4220G>A (BAG6)	XP_011513197.1:n.-13-4220G>A
XM_006715150.3:c.-74C>T (APOM)	XP_006715213.1:n.-74C>T
XM_017011279.2:c.-13-4220G>A (BAG6)	XP_016866768.1:n.-13-4220G>A
XM_024446545.1:c.-14+1768G>A (BAG6)	XP_024302313.1:n.-14+1768G>A
NM_019101.3:c.30C>T (APOM) MANE Select	NP_061974.2:p.Leu10=
NM_001256169.2:c.-102-476C>T (APOM)	NP_001243098.1:n.-102-476C>T
NR_045828.2:n.149-476C>T (APOM)