Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196996046T>C , CM000663.2:g.196996046T>C | GRCh38 |
| NC_000001.10:g.196965176T>C , CM000663.1:g.196965176T>C | GRCh37 |
| NC_000001.9:g.195231799T>C | NCBI36 |
| NG_016365.1:g.23510T>C , LRG_227:g.23510T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.560T>C | ENSP00000514393.1:p.Ile187Thr | |
| ENST00000699467.1:n.884T>C | ||
| ENST00000699468.1:c.-24-68T>C | ENSP00000514394.1:n.-24-68T>C | |
| ENST00000256785.5:c.815T>C MANE Select | ENSP00000256785.4:p.Ile272Thr | |
| ENST00000256785.4:c.815T>C | ENSP00000256785.4:p.Ile272Thr | |
| NM_030787.3:c.815T>C , LRG_227t1:c.815T>C | NP_110414.1:p.Ile272Thr | |
| XM_011510020.1:c.824T>C | XP_011508322.1:p.Ile275Thr | |
| XM_011510020.2:c.824T>C | XP_011508322.1:p.Ile275Thr | |
| NM_030787.4:c.815T>C MANE Select | NP_110414.1:p.Ile272Thr |