Canonical Allele Identifier: CA449666876

Linked Data

MyVariant Identifiers: chr6:g.31625005A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657228A>G , CM000668.2:g.31657228A>G GRCh38
NC_000006.11:g.31625005A>G , CM000668.1:g.31625005A>G GRCh37
NC_000006.10:g.31732984A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.273A>G (APOM) MANE Select ENSP00000365081.3:p.Lys91=
ENST00000375916.3:c.273A>G (APOM) ENSP00000365081.3:p.Lys91=
ENST00000375918.6:c.57A>G (APOM) ENSP00000365083.2:p.Lys19=
ENST00000375920.8:c.57A>G (APOM) ENSP00000365085.4:p.Lys19=
NM_001256169.1:c.57A>G (APOM) NP_001243098.1:p.Lys19=
NM_019101.2:c.273A>G (APOM) NP_061974.2:p.Lys91=
NR_045828.1:n.308A>G (APOM)
XM_006715150.2:c.177A>G (APOM) XP_006715213.1:p.Lys59=
XM_011514895.1:c.-14+3093T>C (BAG6) XP_011513197.1:n.-14+3093T>C
XM_006715150.3:c.177A>G (APOM) XP_006715213.1:p.Lys59=
XM_017011279.2:c.-14+3093T>C (BAG6) XP_016866768.1:n.-14+3093T>C
XM_024446545.1:c.-14+536T>C (BAG6) XP_024302313.1:n.-14+536T>C
NM_019101.3:c.273A>G (APOM) MANE Select NP_061974.2:p.Lys91=
NM_001256169.2:c.57A>G (APOM) NP_001243098.1:p.Lys19=
NR_045828.2:n.314A>G (APOM)