Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7528222T>C , CM000681.2:g.7528222T>C | GRCh38 |
| NC_000019.9:g.7593108T>C , CM000681.1:g.7593108T>C | GRCh37 |
| NC_000019.8:g.7499108T>C | NCBI36 |
| NG_015806.1:g.10613T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.842T>C MANE Select | ENSP00000264079.5:p.Ile281Thr | |
| ENST00000264079.10:c.842T>C | ENSP00000264079.5:p.Ile281Thr | |
| ENST00000394321.9:n.1157T>C | ||
| NM_020533.2:c.842T>C | NP_065394.1:p.Ile281Thr | |
| NM_020533.3:c.842T>C MANE Select | NP_065394.1:p.Ile281Thr |