Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562855T= , CM000682.2:g.57562855T= | GRCh38 |
| NC_000020.10:g.56137911T= , CM000682.1:g.56137911T= | GRCh37 |
| NC_000020.9:g.55571317T= | NCBI36 |
| NG_008205.1:g.6775T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.566T= MANE Select | ENSP00000319814.4:p.Phe189= | |
| ENST00000319441.5:c.566T= | ENSP00000319814.4:p.Phe189= | |
| ENST00000467047.1:n.1776T= | ||
| ENST00000470051.1:n.22T= | ||
| ENST00000498194.1:n.508T= | ||
| NM_002591.3:c.566T= | NP_002582.3:p.Phe189= | |
| XM_011528839.1:c.170T= | XP_011527141.1:p.Phe57= | |
| XM_024451888.1:c.170T= | XP_024307656.1:p.Phe57= | |
| NM_002591.4:c.566T= MANE Select | NP_002582.3:p.Phe189= |