Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128843528T>C , CM000669.2:g.128843528T>C | GRCh38 |
| NC_000007.13:g.128483582T>C , CM000669.1:g.128483582T>C | GRCh37 |
| NC_000007.12:g.128270818T>C | NCBI36 |
| NG_011807.1:g.18100T>C , LRG_870:g.18100T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.2762T>C MANE Select | ENSP00000327145.8:p.Ile921Thr | |
| ENST00000325888.12:c.2762T>C | ENSP00000327145.8:p.Ile921Thr | |
| ENST00000346177.6:c.2762T>C | ENSP00000344002.6:p.Ile921Thr | |
| NM_001127487.1:c.2762T>C | NP_001120959.1:p.Ile921Thr | |
| NM_001458.4:c.2762T>C , LRG_870t1:c.2762T>C | NP_001449.3:p.Ile921Thr | |
| NM_001127487.2:c.2762T>C | NP_001120959.1:p.Ile921Thr | |
| NM_001458.5:c.2762T>C MANE Select | NP_001449.3:p.Ile921Thr |