Canonical Allele Identifier: CA449666898

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1444370457
• gnomAD v3: 6-31657246-C-T
• gnomAD v4: 6-31657246-C-T
• MyVariant Identifiers: chr6:g.31625023C>T (hg19) ; chr6:g.31657246C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657246C>T , CM000668.2:g.31657246C>T	GRCh38
NC_000006.11:g.31625023C>T , CM000668.1:g.31625023C>T	GRCh37
NC_000006.10:g.31733002C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.291C>T (APOM) MANE Select	ENSP00000365081.3:p.Pro97=
ENST00000375916.3:c.291C>T (APOM)	ENSP00000365081.3:p.Pro97=
ENST00000375918.6:c.75C>T (APOM)	ENSP00000365083.2:p.Pro25=
ENST00000375920.8:c.75C>T (APOM)	ENSP00000365085.4:p.Pro25=
NM_001256169.1:c.75C>T (APOM)	NP_001243098.1:p.Pro25=
NM_019101.2:c.291C>T (APOM)	NP_061974.2:p.Pro97=
NR_045828.1:n.326C>T (APOM)
XM_006715150.2:c.195C>T (APOM)	XP_006715213.1:p.Pro65=
XM_011514895.1:c.-14+3075G>A (BAG6)	XP_011513197.1:n.-14+3075G>A
XM_006715150.3:c.195C>T (APOM)	XP_006715213.1:p.Pro65=
XM_017011279.2:c.-14+3075G>A (BAG6)	XP_016866768.1:n.-14+3075G>A
XM_024446545.1:c.-14+518G>A (BAG6)	XP_024302313.1:n.-14+518G>A
NM_019101.3:c.291C>T (APOM) MANE Select	NP_061974.2:p.Pro97=
NM_001256169.2:c.75C>T (APOM)	NP_001243098.1:p.Pro25=
NR_045828.2:n.332C>T (APOM)