Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868975T>C , CM000664.2:g.240868975T>C | GRCh38 |
| NC_000002.11:g.241808392T>C , CM000664.1:g.241808392T>C | GRCh37 |
| NC_000002.10:g.241457065T>C | NCBI36 |
| NG_008005.1:g.5231T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.110T>C MANE Select | ENSP00000302620.3:p.Ile37Thr | |
| ENST00000307503.3:c.110T>C | ENSP00000302620.3:p.Ile37Thr | |
| ENST00000472436.1:n.130T>C | ||
| NM_000030.2:c.110T>C | NP_000021.1:p.Ile37Thr | |
| XR_924060.1:n.405+1258A>G | ||
| NM_000030.3:c.110T>C MANE Select | NP_000021.1:p.Ile37Thr |