Canonical Allele Identifier: CA449666890

Linked Data

MyVariant Identifiers: chr6:g.31625014C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657237C>T , CM000668.2:g.31657237C>T GRCh38
NC_000006.11:g.31625014C>T , CM000668.1:g.31625014C>T GRCh37
NC_000006.10:g.31732993C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.282C>T (APOM) MANE Select ENSP00000365081.3:p.Leu94=
ENST00000375916.3:c.282C>T ENSP00000365081.3:p.Leu94=
ENST00000375918.6:c.66C>T ENSP00000365083.2:p.Leu22=
ENST00000375920.8:c.66C>T ENSP00000365085.4:p.Leu22=
NM_001256169.1:c.66C>T (APOM) NP_001243098.1:p.Leu22=
NM_019101.2:c.282C>T (APOM) NP_061974.2:p.Leu94=
NR_045828.1:n.317C>T (APOM)
XM_006715150.2:c.186C>T (APOM) XP_006715213.1:p.Leu62=
XM_011514895.1:c.-14+3084G>A (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.186C>T (APOM) XP_006715213.1:p.Leu62=
XM_017011279.2:c.-14+3084G>A (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+527G>A (BAG6) XP_024302313.1:p.=
NM_019101.3:c.282C>T (APOM) MANE Select NP_061974.2:p.Leu94=
NM_001256169.2:c.66C>T (APOM) NP_001243098.1:p.Leu22=
NR_045828.2:n.323C>T (APOM)