Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215766759T>G , CM000663.2:g.215766759T>G | GRCh38 |
| NC_000001.10:g.215940101T>G , CM000663.1:g.215940101T>G | GRCh37 |
| NC_000001.9:g.214006724T>G | NCBI36 |
| NG_009497.1:g.661638A>C | |
| NG_009497.2:g.661690A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.10969A>C MANE Select | ENSP00000305941.3:p.Thr3657Pro | |
| ENST00000674083.1:c.10969A>C | ENSP00000501296.1:p.Thr3657Pro | |
| ENST00000307340.7:c.10969A>C | ENSP00000305941.3:p.Thr3657Pro | |
| NM_206933.2:c.10969A>C | NP_996816.2:p.Thr3657Pro | |
| NM_206933.3:c.10969A>C | NP_996816.2:p.Thr3657Pro | |
| NM_206933.4:c.10969A>C MANE Select | NP_996816.3:p.Thr3657Pro |