Canonical Allele Identifier: CA1619249279

Linked Data

dbSNP Id: rs1799481081

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31653860A>T , CM000668.2:g.31653860A>T GRCh38
NC_000006.11:g.31621637A>T , CM000668.1:g.31621637A>T GRCh37
NC_000006.10:g.31729616A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375918.6:c.-103+1309A>T (APOM) ENSP00000365083.2:n.-103+1309A>T
ENST00000375920.8:c.-103+1309A>T (APOM) ENSP00000365085.4:n.-103+1309A>T
NM_001256169.1:c.-103+1309A>T (APOM) NP_001243098.1:n.-103+1309A>T
NR_045828.1:n.142+1309A>T (APOM)
XM_011514895.1:c.-13-2084T>A (BAG6) XP_011513197.1:n.-13-2084T>A
XM_017011279.2:c.-13-2084T>A (BAG6) XP_016866768.1:n.-13-2084T>A
XM_024446545.1:c.-13-2084T>A (BAG6) XP_024302313.1:n.-13-2084T>A
NM_001256169.2:c.-103+1309A>T (APOM) NP_001243098.1:n.-103+1309A>T
NR_045828.2:n.148+1309A>T (APOM)