Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562910T= , CM000682.2:g.57562910T= | GRCh38 |
| NC_000020.10:g.56137966T= , CM000682.1:g.56137966T= | GRCh37 |
| NC_000020.9:g.55571372T= | NCBI36 |
| NG_008205.1:g.6830T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.610+11T= MANE Select | ENSP00000319814.4:n.610+11T= | |
| ENST00000319441.5:c.610+11T= | ENSP00000319814.4:n.610+11T= | |
| ENST00000467047.1:n.1831T= | ||
| ENST00000470051.1:n.77T= | ||
| ENST00000498194.1:n.552+11T= | ||
| NM_002591.3:c.610+11T= | NP_002582.3:n.610+11T= | |
| XM_011528839.1:c.214+11T= | XP_011527141.1:n.214+11T= | |
| XM_024451888.1:c.214+11T= | XP_024307656.1:n.214+11T= | |
| NM_002591.4:c.610+11T= MANE Select | NP_002582.3:n.610+11T= |