Canonical Allele Identifier: CA363427058

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657258C>G , CM000668.2:g.31657258C>G GRCh38
NC_000006.11:g.31625035C>G , CM000668.1:g.31625035C>G GRCh37
NC_000006.10:g.31733014C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.303C>G (APOM) MANE Select ENSP00000365081.3:p.Ile101Met
ENST00000375916.3:c.303C>G (APOM) ENSP00000365081.3:p.Ile101Met
ENST00000375918.6:c.87C>G (APOM) ENSP00000365083.2:p.Ile29Met
ENST00000375920.8:c.87C>G (APOM) ENSP00000365085.4:p.Ile29Met
NM_001256169.1:c.87C>G (APOM) NP_001243098.1:p.Ile29Met
NM_019101.2:c.303C>G (APOM) NP_061974.2:p.Ile101Met
NR_045828.1:n.338C>G (APOM)
XM_006715150.2:c.207C>G (APOM) XP_006715213.1:p.Ile69Met
XM_011514895.1:c.-14+3063G>C (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.207C>G (APOM) XP_006715213.1:p.Ile69Met
XM_017011279.2:c.-14+3063G>C (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+506G>C (BAG6) XP_024302313.1:p.=
NM_019101.3:c.303C>G (APOM) MANE Select NP_061974.2:p.Ile101Met
NM_001256169.2:c.87C>G (APOM) NP_001243098.1:p.Ile29Met
NR_045828.2:n.344C>G (APOM)