Canonical Allele Identifier: CA1619249984
Community Standard Title: NC_000006.12:g.31655639G=

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31655639G= , CM000668.2:g.31655639G= GRCh38
NC_000006.11:g.31623416G= , CM000668.1:g.31623416G= GRCh37
NC_000006.10:g.31731395G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001256169.1:c.-102-833G= (APOM) NP_001243098.1:n.-102-833G=
NM_001256169.2:c.-102-833G= (APOM) NP_001243098.1:n.-102-833G=
NR_045828.1:n.143-833G= (APOM)
NR_045828.2:n.149-833G= (APOM)
ENST00000375916.3:c.-328G= (APOM) ENSP00000365081.3:n.-328G=
ENST00000375918.6:c.-102-833G= (APOM) ENSP00000365083.2:n.-102-833G=
ENST00000375920.8:c.-102-833G= (APOM) ENSP00000365085.4:n.-102-833G=
XM_006715150.2:c.-431G= (APOM) XP_006715213.1:n.-431G=
XM_011514895.1:c.-13-3863C= (BAG6) XP_011513197.1:n.-13-3863C=
XM_017011279.2:c.-13-3863C= (BAG6) XP_016866768.1:n.-13-3863C=
XM_024446545.1:c.-14+2125C= (BAG6) XP_024302313.1:n.-14+2125C=