Canonical Allele Identifier: CA449666882

Linked Data

MyVariant Identifiers: chr6:g.31625011G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657234G>A , CM000668.2:g.31657234G>A GRCh38
NC_000006.11:g.31625011G>A , CM000668.1:g.31625011G>A GRCh37
NC_000006.10:g.31732990G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.279G>A (APOM) MANE Select ENSP00000365081.3:p.Gly93=
ENST00000375916.3:c.279G>A (APOM) ENSP00000365081.3:p.Gly93=
ENST00000375918.6:c.63G>A (APOM) ENSP00000365083.2:p.Gly21=
ENST00000375920.8:c.63G>A (APOM) ENSP00000365085.4:p.Gly21=
NM_001256169.1:c.63G>A (APOM) NP_001243098.1:p.Gly21=
NM_019101.2:c.279G>A (APOM) NP_061974.2:p.Gly93=
NR_045828.1:n.314G>A (APOM)
XM_006715150.2:c.183G>A (APOM) XP_006715213.1:p.Gly61=
XM_011514895.1:c.-14+3087C>T (BAG6) XP_011513197.1:n.-14+3087C>T
XM_006715150.3:c.183G>A (APOM) XP_006715213.1:p.Gly61=
XM_017011279.2:c.-14+3087C>T (BAG6) XP_016866768.1:n.-14+3087C>T
XM_024446545.1:c.-14+530C>T (BAG6) XP_024302313.1:n.-14+530C>T
NM_019101.3:c.279G>A (APOM) MANE Select NP_061974.2:p.Gly93=
NM_001256169.2:c.63G>A (APOM) NP_001243098.1:p.Gly21=
NR_045828.2:n.320G>A (APOM)