Canonical Allele Identifier: CA136879937

Linked Data

dbSNP Id: rs9267528

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31654364C>T , CM000668.2:g.31654364C>T GRCh38
NC_000006.11:g.31622141C>T , CM000668.1:g.31622141C>T GRCh37
NC_000006.10:g.31730120C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375918.6:c.-103+1813C>T ENSP00000365083.2:p.=
ENST00000375920.8:c.-103+1813C>T ENSP00000365085.4:p.=
NM_001256169.1:c.-103+1813C>T (APOM) NP_001243098.1:p.=
NR_045828.1:n.142+1813C>T (APOM)
XM_011514895.1:c.-13-2588G>A (BAG6) XP_011513197.1:p.=
XM_017011279.2:c.-13-2588G>A (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-13-2588G>A (BAG6) XP_024302313.1:p.=
NM_001256169.2:c.-103+1813C>T (APOM) NP_001243098.1:p.=
NR_045828.2:n.148+1813C>T (APOM)