Linked Data
gnomAD v4:
5-159320326-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320326C>G , CM000667.2:g.159320326C>G | GRCh38 |
| NC_000005.9:g.158747334C>G , CM000667.1:g.158747334C>G | GRCh37 |
| NC_000005.8:g.158679912C>G | NCBI36 |
| NG_009618.1:g.15148G>C , LRG_71:g.15148G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.47G>C | ENSP00000512849.1:p.Ser16Thr | |
| ENST00000696751.1:c.*172G>C | ENSP00000512850.1:n.*172G>C | |
| ENST00000231228.3:c.677G>C MANE Select | ENSP00000231228.2:p.Ser226Thr | |
| ENST00000231228.2:c.677G>C | ENSP00000231228.2:p.Ser226Thr | |
| NM_002187.2:c.677G>C , LRG_71t1:c.677G>C | NP_002178.2:p.Ser226Thr | |
| NM_002187.3:c.677G>C MANE Select | NP_002178.2:p.Ser226Thr |