Canonical Allele Identifier: CA2594637226

Linked Data

dbSNP Id: rs2151131321

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31653969dup , CM000668.2:g.31653969dup GRCh38
NC_000006.11:g.31621746dup , CM000668.1:g.31621746dup GRCh37
NC_000006.10:g.31729725dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375918.6:c.-103+1418dup (APOM) ENSP00000365083.2:n.-103+1418dup
ENST00000375920.8:c.-103+1418dup (APOM) ENSP00000365085.4:n.-103+1418dup
NM_001256169.1:c.-103+1418dup (APOM) NP_001243098.1:n.-103+1418dup
NR_045828.1:n.142+1418dup (APOM)
XM_011514895.1:c.-13-2193dup (BAG6) XP_011513197.1:n.-13-2193dup
XM_017011279.2:c.-13-2193dup (BAG6) XP_016866768.1:n.-13-2193dup
XM_024446545.1:c.-13-2193dup (BAG6) XP_024302313.1:n.-13-2193dup
NM_001256169.2:c.-103+1418dup (APOM) NP_001243098.1:n.-103+1418dup
NR_045828.2:n.148+1418dup (APOM)