Canonical Allele Identifier: CA449666883

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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