Canonical Allele Identifier: CA363426912

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657242T>G , CM000668.2:g.31657242T>G GRCh38
NC_000006.11:g.31625019T>G , CM000668.1:g.31625019T>G GRCh37
NC_000006.10:g.31732998T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.287T>G (APOM) MANE Select ENSP00000365081.3:p.Val96Gly
ENST00000375916.3:c.287T>G ENSP00000365081.3:p.Val96Gly
ENST00000375918.6:c.71T>G ENSP00000365083.2:p.Val24Gly
ENST00000375920.8:c.71T>G ENSP00000365085.4:p.Val24Gly
NM_001256169.1:c.71T>G (APOM) NP_001243098.1:p.Val24Gly
NM_019101.2:c.287T>G (APOM) NP_061974.2:p.Val96Gly
NR_045828.1:n.322T>G (APOM)
XM_006715150.2:c.191T>G (APOM) XP_006715213.1:p.Val64Gly
XM_011514895.1:c.-14+3079A>C (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.191T>G (APOM) XP_006715213.1:p.Val64Gly
XM_017011279.2:c.-14+3079A>C (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+522A>C (BAG6) XP_024302313.1:p.=
NM_019101.3:c.287T>G (APOM) MANE Select NP_061974.2:p.Val96Gly
NM_001256169.2:c.71T>G (APOM) NP_001243098.1:p.Val24Gly
NR_045828.2:n.328T>G (APOM)