Canonical Allele Identifier: CA2677982318

Linked Data

gnomAD v4: 6-31655774-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31655774C>A , CM000668.2:g.31655774C>A GRCh38
NC_000006.11:g.31623551C>A , CM000668.1:g.31623551C>A GRCh37
NC_000006.10:g.31731530C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.3:c.-193C>A (APOM) ENSP00000365081.3:n.-193C>A
ENST00000375918.6:c.-102-698C>A (APOM) ENSP00000365083.2:n.-102-698C>A
ENST00000375920.8:c.-102-698C>A (APOM) ENSP00000365085.4:n.-102-698C>A
NM_001256169.1:c.-102-698C>A (APOM) NP_001243098.1:n.-102-698C>A
NR_045828.1:n.143-698C>A (APOM)
XM_006715150.2:c.-296C>A (APOM) XP_006715213.1:n.-296C>A
XM_011514895.1:c.-13-3998G>T (BAG6) XP_011513197.1:n.-13-3998G>T
XM_017011279.2:c.-13-3998G>T (BAG6) XP_016866768.1:n.-13-3998G>T
XM_024446545.1:c.-14+1990G>T (BAG6) XP_024302313.1:n.-14+1990G>T
NM_001256169.2:c.-102-698C>A (APOM) NP_001243098.1:n.-102-698C>A
NR_045828.2:n.149-698C>A (APOM)