Linked Data
dbSNP Id:
rs1000769980
gnomAD v2:
7-150036611-T-C
gnomAD v3:
7-150339522-T-C
gnomAD v4:
7-150339522-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150339522T>C , CM000669.2:g.150339522T>C | GRCh38 |
| NC_000007.13:g.150036611T>C , CM000669.1:g.150036611T>C | GRCh37 |
| NC_000007.12:g.149667544T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000223271.8:c.280-441A>G MANE Select | ENSP00000223271.3:n.280-441A>G | |
| ENST00000223271.7:c.280-441A>G | ENSP00000223271.3:n.280-441A>G | |
| ENST00000466675.5:c.280-441A>G | ENSP00000418009.1:n.280-441A>G | |
| ENST00000467793.5:c.280-441A>G | ENSP00000417669.1:n.280-441A>G | |
| ENST00000478771.2:n.1562-441A>G | ||
| ENST00000482669.1:c.280-441A>G | ENSP00000418483.1:n.280-441A>G | |
| NM_002889.3:c.280-441A>G | NP_002880.1:n.280-441A>G | |
| XM_017012491.1:c.280-441A>G | XP_016867980.1:n.280-441A>G | |
| NM_002889.4:c.280-441A>G MANE Select | NP_002880.1:n.280-441A>G |