Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188994064T= , CM000664.2:g.188994064T= | GRCh38 |
| NC_000002.11:g.189858790T= , CM000664.1:g.189858790T= | GRCh37 |
| NC_000002.10:g.189567035T= | NCBI36 |
| NG_007404.1:g.24692T= , LRG_3:g.24692T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.1077T= | ENSP00000415346.2:p.Pro359= | |
| ENST00000304636.9:c.1176T= MANE Select | ENSP00000304408.4:p.Pro392= | |
| ENST00000304636.7:c.1176T= | ENSP00000304408.3:p.Pro392= | |
| ENST00000317840.9:c.1176T= | ENSP00000315243.6:p.Pro392= | |
| ENST00000450867.1:c.175T= | ||
| NM_000090.3:c.1176T= , LRG_3t1:c.1176T= | NP_000081.1:p.Pro392= | |
| NM_000090.4:c.1176T= MANE Select | NP_000081.2:p.Pro392= |