Canonical Allele Identifier: CA449666903

Linked Data

MyVariant Identifiers: chr6:g.31625026G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657249G>C , CM000668.2:g.31657249G>C GRCh38
NC_000006.11:g.31625026G>C , CM000668.1:g.31625026G>C GRCh37
NC_000006.10:g.31733005G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.294G>C (APOM) MANE Select ENSP00000365081.3:p.Arg98=
ENST00000375916.3:c.294G>C (APOM) ENSP00000365081.3:p.Arg98=
ENST00000375918.6:c.78G>C (APOM) ENSP00000365083.2:p.Arg26=
ENST00000375920.8:c.78G>C (APOM) ENSP00000365085.4:p.Arg26=
NM_001256169.1:c.78G>C (APOM) NP_001243098.1:p.Arg26=
NM_019101.2:c.294G>C (APOM) NP_061974.2:p.Arg98=
NR_045828.1:n.329G>C (APOM)
XM_006715150.2:c.198G>C (APOM) XP_006715213.1:p.Arg66=
XM_011514895.1:c.-14+3072C>G (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.198G>C (APOM) XP_006715213.1:p.Arg66=
XM_017011279.2:c.-14+3072C>G (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+515C>G (BAG6) XP_024302313.1:p.=
NM_019101.3:c.294G>C (APOM) MANE Select NP_061974.2:p.Arg98=
NM_001256169.2:c.78G>C (APOM) NP_001243098.1:p.Arg26=
NR_045828.2:n.335G>C (APOM)