Canonical Allele Identifier: CA136879992
Gene: APOM HGNC NCBI
BAG6 HGNC NCBI

Linked Data

dbSNP Id: rs55880811
MyVariant Identifiers: chr6:g.31622531T>C (hg19) chr6:g.31654754T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31654754T>C , CM000668.2:g.31654754T>C GRCh38
NC_000006.11:g.31622531T>C , CM000668.1:g.31622531T>C GRCh37
NC_000006.10:g.31730510T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375918.6:c.-102-1718T>C (APOM) ENSP00000365083.2:n.-102-1718T>C
ENST00000375920.8:c.-102-1718T>C (APOM) ENSP00000365085.4:n.-102-1718T>C
NM_001256169.1:c.-102-1718T>C (APOM) NP_001243098.1:n.-102-1718T>C
NR_045828.1:n.143-1718T>C (APOM)
XM_011514895.1:c.-13-2978A>G (BAG6) XP_011513197.1:n.-13-2978A>G
XM_017011279.2:c.-13-2978A>G (BAG6) XP_016866768.1:n.-13-2978A>G
XM_024446545.1:c.-13-2978A>G (BAG6) XP_024302313.1:n.-13-2978A>G
NM_001256169.2:c.-102-1718T>C (APOM) NP_001243098.1:n.-102-1718T>C
NR_045828.2:n.149-1718T>C (APOM)
Search 100 bp 5'
Search 100 bp 3'