Allele Registry

Canonical Allele Identifier: CA15438616

Gene: APOM HGNC NCBI
BAG6 HGNC NCBI

Linked Data - Expert Curation

COSMIC:

COSN17138864 (not active)

COSN17148208 (not active)

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr6:g.31652743T>G

GRCh37 chr6:g.31620520T>G

Linked Data - Sequence & Population

gnomAD v2:

6:31620520 T / G

gnomAD v3:

6:31652743 T / G

gnomAD v4:

chr6-31652743-T-G

Joint Max Group AF 0.10531701 (NFE)

Genomes Max Group AF 0.10561259 (NFE)

Exomes Max Group AF 0.05393397 (NFE)

Linked Data - NCBI & NCI

dbSNP:

3117582

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31652743T>G , CM000668.2:g.31652743T>G	GRCh38
NC_000006.11:g.31620520T>G , CM000668.1:g.31620520T>G	GRCh37
NC_000006.10:g.31728499T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375918.6:c.-103+192T>G (APOM)	ENSP00000365083.2:n.-103+192T>G
ENST00000375920.8:c.-103+192T>G (APOM)	ENSP00000365085.4:n.-103+192T>G
NM_001256169.1:c.-103+192T>G (APOM)	NP_001243098.1:n.-103+192T>G
NR_045828.1:n.142+192T>G (APOM)
XM_011514892.1:c.-333A>C (BAG6)	XP_011513194.1:n.-333A>C
XM_011514895.1:c.-13-967A>C (BAG6)	XP_011513197.1:n.-13-967A>C
XM_011514900.1:c.-333A>C (BAG6)	XP_011513202.1:n.-333A>C
XM_017011279.2:c.-13-967A>C (BAG6)	XP_016866768.1:n.-13-967A>C
XM_024446545.1:c.-13-967A>C (BAG6)	XP_024302313.1:n.-13-967A>C
NM_001256169.2:c.-103+192T>G (APOM)	NP_001243098.1:n.-103+192T>G
NR_045828.2:n.148+192T>G (APOM)

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