Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65170135G>C , CM000674.2:g.65170135G>C | GRCh38 |
| NC_000012.11:g.65563915G>C , CM000674.1:g.65563915G>C | GRCh37 |
| NC_000012.10:g.63850182G>C | NCBI36 |
| NG_016210.1:g.5565G>C | |
| NG_016210.2:g.5565G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.539G>C MANE Select | ENSP00000308369.2:p.Ser180Thr | |
| ENST00000308330.2:c.539G>C | ENSP00000308369.2:p.Ser180Thr | |
| ENST00000541171.1:n.553G>C | ||
| NM_001167614.1:c.539G>C | NP_001161086.1:p.Ser180Thr | |
| NM_014319.4:c.539G>C | NP_055134.2:p.Ser180Thr | |
| NM_014319.5:c.539G>C MANE Select | NP_055134.2:p.Ser180Thr | |
| NM_001167614.2:c.539G>C | NP_001161086.1:p.Ser180Thr |