Linked Data
dbSNP Id:
rs1334323968
gnomAD v2:
6-31623691-T-G
gnomAD v3:
6-31655914-T-G
gnomAD v4:
6-31655914-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31655914T>G , CM000668.2:g.31655914T>G | GRCh38 |
| NC_000006.11:g.31623691T>G , CM000668.1:g.31623691T>G | GRCh37 |
| NC_000006.10:g.31731670T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375916.4:c.-53T>G (APOM) MANE Select | ENSP00000365081.3:n.-53T>G | |
| ENST00000375916.3:c.-53T>G (APOM) | ENSP00000365081.3:n.-53T>G | |
| ENST00000375918.6:c.-102-558T>G (APOM) | ENSP00000365083.2:n.-102-558T>G | |
| ENST00000375920.8:c.-102-558T>G (APOM) | ENSP00000365085.4:n.-102-558T>G | |
| NM_001256169.1:c.-102-558T>G (APOM) | NP_001243098.1:n.-102-558T>G | |
| NM_019101.2:c.-53T>G (APOM) | NP_061974.2:n.-53T>G | |
| NR_045828.1:n.143-558T>G (APOM) | ||
| XM_006715150.2:c.-156T>G (APOM) | XP_006715213.1:n.-156T>G | |
| XM_011514895.1:c.-13-4138A>C (BAG6) | XP_011513197.1:n.-13-4138A>C | |
| XM_017011279.2:c.-13-4138A>C (BAG6) | XP_016866768.1:n.-13-4138A>C | |
| XM_024446545.1:c.-14+1850A>C (BAG6) | XP_024302313.1:n.-14+1850A>C | |
| NM_019101.3:c.-53T>G (APOM) MANE Select | NP_061974.2:n.-53T>G | |
| NM_001256169.2:c.-102-558T>G (APOM) | NP_001243098.1:n.-102-558T>G | |
| NR_045828.2:n.149-558T>G (APOM) |