Canonical Allele Identifier: CA1619249700
Gene: APOM HGNC NCBI
BAG6 HGNC NCBI

Linked Data

dbSNP Id: rs1799870758
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31654910A>G , CM000668.2:g.31654910A>G GRCh38
NC_000006.11:g.31622687A>G , CM000668.1:g.31622687A>G GRCh37
NC_000006.10:g.31730666A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375918.6:c.-102-1562A>G (APOM) ENSP00000365083.2:n.-102-1562A>G
ENST00000375920.8:c.-102-1562A>G (APOM) ENSP00000365085.4:n.-102-1562A>G
NM_001256169.1:c.-102-1562A>G (APOM) NP_001243098.1:n.-102-1562A>G
NR_045828.1:n.143-1562A>G (APOM)
XM_011514895.1:c.-13-3134T>C (BAG6) XP_011513197.1:n.-13-3134T>C
XM_017011279.2:c.-13-3134T>C (BAG6) XP_016866768.1:n.-13-3134T>C
XM_024446545.1:c.-14+2854T>C (BAG6) XP_024302313.1:n.-14+2854T>C
NM_001256169.2:c.-102-1562A>G (APOM) NP_001243098.1:n.-102-1562A>G
NR_045828.2:n.149-1562A>G (APOM)
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