Linked Data
dbSNP Id:
rs766115049
ExAC:
11:67352605 C / T
gnomAD v2:
11-67352605-C-T
gnomAD v4:
11-67585134-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585134C>T , CM000673.2:g.67585134C>T | GRCh38 |
| NC_000011.9:g.67352605C>T , CM000673.1:g.67352605C>T | GRCh37 |
| NC_000011.8:g.67109181C>T | NCBI36 |
| NG_012075.1:g.6540C>T , LRG_723:g.6540C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000398603.6:c.233-4C>T | ENSP00000381604.1:n.233-4C>T | |
| ENST00000398606.10:c.233-4C>T MANE Select | ENSP00000381607.3:n.233-4C>T | |
| ENST00000646888.1:c.126-4C>T | ENSP00000494477.1:n.126-4C>T | |
| ENST00000398603.5:c.233-4C>T | ENSP00000381604.1:n.233-4C>T | |
| ENST00000398606.7:c.233-4C>T | ENSP00000381607.3:n.233-4C>T | |
| ENST00000467591.1:n.340C>T | ||
| ENST00000494593.1:n.1024C>T | ||
| ENST00000498765.5:c.292C>T | ||
| NM_000852.3:c.233-4C>T , LRG_723t1:c.233-4C>T | NP_000843.1:n.233-4C>T | |
| NM_000852.4:c.233-4C>T MANE Select | NP_000843.1:n.233-4C>T |