Canonical Allele Identifier: CA1087476300

Linked Data

dbSNP Id: rs1799865439
gnomAD v3: 6-31654863-G-C
gnomAD v4: 6-31654863-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31654863G>C , CM000668.2:g.31654863G>C GRCh38
NC_000006.11:g.31622640G>C , CM000668.1:g.31622640G>C GRCh37
NC_000006.10:g.31730619G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375918.6:c.-102-1609G>C (APOM) ENSP00000365083.2:n.-102-1609G>C
ENST00000375920.8:c.-102-1609G>C (APOM) ENSP00000365085.4:n.-102-1609G>C
NM_001256169.1:c.-102-1609G>C (APOM) NP_001243098.1:n.-102-1609G>C
NR_045828.1:n.143-1609G>C (APOM)
XM_011514895.1:c.-13-3087C>G (BAG6) XP_011513197.1:n.-13-3087C>G
XM_017011279.2:c.-13-3087C>G (BAG6) XP_016866768.1:n.-13-3087C>G
XM_024446545.1:c.-14+2901C>G (BAG6) XP_024302313.1:n.-14+2901C>G
NM_001256169.2:c.-102-1609G>C (APOM) NP_001243098.1:n.-102-1609G>C
NR_045828.2:n.149-1609G>C (APOM)