Canonical Allele Identifier: CA566362870

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1156531461
• gnomAD v2: 6-31621799-G-A
• gnomAD v3: 6-31654022-G-A
• gnomAD v4: 6-31654022-G-A
• MyVariant Identifiers: chr6:g.31621799G>A (hg19) ; chr6:g.31654022G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31654022G>A , CM000668.2:g.31654022G>A	GRCh38
NC_000006.11:g.31621799G>A , CM000668.1:g.31621799G>A	GRCh37
NC_000006.10:g.31729778G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375918.6:c.-103+1471G>A (APOM)	ENSP00000365083.2:n.-103+1471G>A
ENST00000375920.8:c.-103+1471G>A (APOM)	ENSP00000365085.4:n.-103+1471G>A
NM_001256169.1:c.-103+1471G>A (APOM)	NP_001243098.1:n.-103+1471G>A
NR_045828.1:n.142+1471G>A (APOM)
XM_011514895.1:c.-13-2246C>T (BAG6)	XP_011513197.1:n.-13-2246C>T
XM_017011279.2:c.-13-2246C>T (BAG6)	XP_016866768.1:n.-13-2246C>T
XM_024446545.1:c.-13-2246C>T (BAG6)	XP_024302313.1:n.-13-2246C>T
NM_001256169.2:c.-103+1471G>A (APOM)	NP_001243098.1:n.-103+1471G>A
NR_045828.2:n.148+1471G>A (APOM)