Canonical Allele Identifier: CA136880089
Gene: APOM HGNC NCBI
BAG6 HGNC NCBI

Linked Data

dbSNP Id: rs76611345
MyVariant Identifiers: chr6:g.31623074C>A (hg19) chr6:g.31655297C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31655297C>A , CM000668.2:g.31655297C>A GRCh38
NC_000006.11:g.31623074C>A , CM000668.1:g.31623074C>A GRCh37
NC_000006.10:g.31731053C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375918.6:c.-102-1175C>A (APOM) ENSP00000365083.2:n.-102-1175C>A
ENST00000375920.8:c.-102-1175C>A (APOM) ENSP00000365085.4:n.-102-1175C>A
NM_001256169.1:c.-102-1175C>A (APOM) NP_001243098.1:n.-102-1175C>A
NR_045828.1:n.143-1175C>A (APOM)
XM_006715150.2:c.-773C>A (APOM) XP_006715213.1:n.-773C>A
XM_011514895.1:c.-13-3521G>T (BAG6) XP_011513197.1:n.-13-3521G>T
XM_017011279.2:c.-13-3521G>T (BAG6) XP_016866768.1:n.-13-3521G>T
XM_024446545.1:c.-14+2467G>T (BAG6) XP_024302313.1:n.-14+2467G>T
NM_001256169.2:c.-102-1175C>A (APOM) NP_001243098.1:n.-102-1175C>A
NR_045828.2:n.149-1175C>A (APOM)
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