Canonical Allele Identifier: CA3717920

Linked Data

dbSNP Id: rs805264

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31656096G>A , CM000668.2:g.31656096G>A GRCh38
NC_000006.11:g.31623873G>A , CM000668.1:g.31623873G>A GRCh37
NC_000006.10:g.31731852G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.114+16G>A (APOM) MANE Select ENSP00000365081.3:p.=
ENST00000375916.3:c.114+16G>A ENSP00000365081.3:p.=
ENST00000375918.6:c.-102-376G>A ENSP00000365083.2:p.=
ENST00000375920.8:c.-102-376G>A ENSP00000365085.4:p.=
NM_001256169.1:c.-102-376G>A (APOM) NP_001243098.1:p.=
NM_019101.2:c.114+16G>A (APOM) NP_061974.2:p.=
NR_045828.1:n.143-376G>A (APOM)
XM_006715150.2:c.11+16G>A (APOM) XP_006715213.1:p.=
XM_011514895.1:c.-14+4225C>T (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.11+16G>A (APOM) XP_006715213.1:p.=
XM_017011279.2:c.-14+4225C>T (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+1668C>T (BAG6) XP_024302313.1:p.=
NM_019101.3:c.114+16G>A (APOM) MANE Select NP_061974.2:p.=
NM_001256169.2:c.-102-376G>A (APOM) NP_001243098.1:p.=
NR_045828.2:n.149-376G>A (APOM)