Canonical Allele Identifier: CA1619250057

Linked Data

dbSNP Id: rs1799980543
gnomAD v4: 6-31655822-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31655822T>G , CM000668.2:g.31655822T>G GRCh38
NC_000006.11:g.31623599T>G , CM000668.1:g.31623599T>G GRCh37
NC_000006.10:g.31731578T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.3:c.-145T>G (APOM) ENSP00000365081.3:n.-145T>G
ENST00000375918.6:c.-102-650T>G (APOM) ENSP00000365083.2:n.-102-650T>G
ENST00000375920.8:c.-102-650T>G (APOM) ENSP00000365085.4:n.-102-650T>G
NM_001256169.1:c.-102-650T>G (APOM) NP_001243098.1:n.-102-650T>G
NR_045828.1:n.143-650T>G (APOM)
XM_006715150.2:c.-248T>G (APOM) XP_006715213.1:n.-248T>G
XM_011514895.1:c.-13-4046A>C (BAG6) XP_011513197.1:n.-13-4046A>C
XM_017011279.2:c.-13-4046A>C (BAG6) XP_016866768.1:n.-13-4046A>C
XM_024446545.1:c.-14+1942A>C (BAG6) XP_024302313.1:n.-14+1942A>C
NM_001256169.2:c.-102-650T>G (APOM) NP_001243098.1:n.-102-650T>G
NR_045828.2:n.149-650T>G (APOM)