Canonical Allele Identifier: CA363426929
Gene: APOM HGNC NCBI
BAG6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31625021C>G (hg19) chr6:g.31657244C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657244C>G , CM000668.2:g.31657244C>G GRCh38
NC_000006.11:g.31625021C>G , CM000668.1:g.31625021C>G GRCh37
NC_000006.10:g.31733000C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.289C>G (APOM) MANE Select ENSP00000365081.3:p.Pro97Ala
ENST00000375916.3:c.289C>G (APOM) ENSP00000365081.3:p.Pro97Ala
ENST00000375918.6:c.73C>G (APOM) ENSP00000365083.2:p.Pro25Ala
ENST00000375920.8:c.73C>G (APOM) ENSP00000365085.4:p.Pro25Ala
NM_001256169.1:c.73C>G (APOM) NP_001243098.1:p.Pro25Ala
NM_019101.2:c.289C>G (APOM) NP_061974.2:p.Pro97Ala
NR_045828.1:n.324C>G (APOM)
XM_006715150.2:c.193C>G (APOM) XP_006715213.1:p.Pro65Ala
XM_011514895.1:c.-14+3077G>C (BAG6) XP_011513197.1:n.-14+3077G>C
XM_006715150.3:c.193C>G (APOM) XP_006715213.1:p.Pro65Ala
XM_017011279.2:c.-14+3077G>C (BAG6) XP_016866768.1:n.-14+3077G>C
XM_024446545.1:c.-14+520G>C (BAG6) XP_024302313.1:n.-14+520G>C
NM_019101.3:c.289C>G (APOM) MANE Select NP_061974.2:p.Pro97Ala
NM_001256169.2:c.73C>G (APOM) NP_001243098.1:p.Pro25Ala
NR_045828.2:n.330C>G (APOM)
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