Canonical Allele Identifier: CA3717975

Linked Data

dbSNP Id: rs778859096

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657247C>T , CM000668.2:g.31657247C>T GRCh38
NC_000006.11:g.31625024C>T , CM000668.1:g.31625024C>T GRCh37
NC_000006.10:g.31733003C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.292C>T (APOM) MANE Select ENSP00000365081.3:p.Arg98Trp
ENST00000375916.3:c.292C>T (APOM) ENSP00000365081.3:p.Arg98Trp
ENST00000375918.6:c.76C>T (APOM) ENSP00000365083.2:p.Arg26Trp
ENST00000375920.8:c.76C>T (APOM) ENSP00000365085.4:p.Arg26Trp
NM_001256169.1:c.76C>T (APOM) NP_001243098.1:p.Arg26Trp
NM_019101.2:c.292C>T (APOM) NP_061974.2:p.Arg98Trp
NR_045828.1:n.327C>T (APOM)
XM_006715150.2:c.196C>T (APOM) XP_006715213.1:p.Arg66Trp
XM_011514895.1:c.-14+3074G>A (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.196C>T (APOM) XP_006715213.1:p.Arg66Trp
XM_017011279.2:c.-14+3074G>A (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+517G>A (BAG6) XP_024302313.1:p.=
NM_019101.3:c.292C>T (APOM) MANE Select NP_061974.2:p.Arg98Trp
NM_001256169.2:c.76C>T (APOM) NP_001243098.1:p.Arg26Trp
NR_045828.2:n.333C>T (APOM)