Canonical Allele Identifier: CA15453312

Linked Data

dbSNP Id: rs805297

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31654829C>A , CM000668.2:g.31654829C>A GRCh38
NC_000006.11:g.31622606C>A , CM000668.1:g.31622606C>A GRCh37
NC_000006.10:g.31730585C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375918.6:c.-102-1643C>A ENSP00000365083.2:p.=
ENST00000375920.8:c.-102-1643C>A ENSP00000365085.4:p.=
NM_001256169.1:c.-102-1643C>A (APOM) NP_001243098.1:p.=
NR_045828.1:n.143-1643C>A (APOM)
XM_011514895.1:c.-13-3053G>T (BAG6) XP_011513197.1:p.=
XM_017011279.2:c.-13-3053G>T (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+2935G>T (BAG6) XP_024302313.1:p.=
NM_001256169.2:c.-102-1643C>A (APOM) NP_001243098.1:p.=
NR_045828.2:n.149-1643C>A (APOM)