Canonical Allele Identifier: CA136880307

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1056737293
• MyVariant Identifiers: chr6:g.31624601C>T (hg19) ; chr6:g.31656824C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656824C>T , CM000668.2:g.31656824C>T	GRCh38
NC_000006.11:g.31624601C>T , CM000668.1:g.31624601C>T	GRCh37
NC_000006.10:g.31732580C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.269+198C>T (APOM) MANE Select	ENSP00000365081.3:n.269+198C>T
ENST00000375916.3:c.269+198C>T (APOM)	ENSP00000365081.3:n.269+198C>T
ENST00000375918.6:c.53+198C>T (APOM)	ENSP00000365083.2:n.53+198C>T
ENST00000375920.8:c.53+198C>T (APOM)	ENSP00000365085.4:n.53+198C>T
NM_001256169.1:c.53+198C>T (APOM)	NP_001243098.1:n.53+198C>T
NM_019101.2:c.269+198C>T (APOM)	NP_061974.2:n.269+198C>T
NR_045828.1:n.304+191C>T (APOM)
XM_006715150.2:c.173+191C>T (APOM)	XP_006715213.1:n.173+191C>T
XM_011514895.1:c.-14+3497G>A (BAG6)	XP_011513197.1:n.-14+3497G>A
XM_006715150.3:c.173+191C>T (APOM)	XP_006715213.1:n.173+191C>T
XM_017011279.2:c.-14+3497G>A (BAG6)	XP_016866768.1:n.-14+3497G>A
XM_024446545.1:c.-14+940G>A (BAG6)	XP_024302313.1:n.-14+940G>A
NM_019101.3:c.269+198C>T (APOM) MANE Select	NP_061974.2:n.269+198C>T
NM_001256169.2:c.53+198C>T (APOM)	NP_001243098.1:n.53+198C>T
NR_045828.2:n.310+191C>T (APOM)