Canonical Allele Identifier: CA1619250074

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31655872C= , CM000668.2:g.31655872C= GRCh38
NC_000006.11:g.31623649C= , CM000668.1:g.31623649C= GRCh37
NC_000006.10:g.31731628C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.3:c.-95C= (APOM) ENSP00000365081.3:n.-95C=
ENST00000375918.6:c.-102-600C= (APOM) ENSP00000365083.2:n.-102-600C=
ENST00000375920.8:c.-102-600C= (APOM) ENSP00000365085.4:n.-102-600C=
NM_001256169.1:c.-102-600C= (APOM) NP_001243098.1:n.-102-600C=
NR_045828.1:n.143-600C= (APOM)
XM_006715150.2:c.-198C= (APOM) XP_006715213.1:n.-198C=
XM_011514895.1:c.-13-4096G= (BAG6) XP_011513197.1:n.-13-4096G=
XM_017011279.2:c.-13-4096G= (BAG6) XP_016866768.1:n.-13-4096G=
XM_024446545.1:c.-14+1892G= (BAG6) XP_024302313.1:n.-14+1892G=
NM_001256169.2:c.-102-600C= (APOM) NP_001243098.1:n.-102-600C=
NR_045828.2:n.149-600C= (APOM)