Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7528833T= , CM000681.2:g.7528833T= | GRCh38 |
| NC_000019.9:g.7593719T= , CM000681.1:g.7593719T= | GRCh37 |
| NC_000019.8:g.7499719T= | NCBI36 |
| NG_015806.1:g.11224T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264079.11:c.997T= MANE Select | ENSP00000264079.5:p.Phe333= | |
| ENST00000264079.10:c.997T= | ENSP00000264079.5:p.Phe333= | |
| ENST00000394321.9:n.1312T= | ||
| ENST00000595860.5:n.180T= | ||
| NM_020533.2:c.997T= | NP_065394.1:p.Phe333= | |
| NM_020533.3:c.997T= MANE Select | NP_065394.1:p.Phe333= |