Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562989G= , CM000682.2:g.57562989G= | GRCh38 |
| NC_000020.10:g.56138045G= , CM000682.1:g.56138045G= | GRCh37 |
| NC_000020.9:g.55571451G= | NCBI36 |
| NG_008205.1:g.6909G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.611-39G= MANE Select | ENSP00000319814.4:n.611-39G= | |
| ENST00000319441.5:c.611-39G= | ENSP00000319814.4:n.611-39G= | |
| ENST00000467047.1:n.1910G= | ||
| ENST00000470051.1:n.156G= | ||
| ENST00000498194.1:n.553-39G= | ||
| NM_002591.3:c.611-39G= | NP_002582.3:n.611-39G= | |
| XM_011528839.1:c.215-39G= | XP_011527141.1:n.215-39G= | |
| XM_024451888.1:c.215-39G= | XP_024307656.1:n.215-39G= | |
| NM_002591.4:c.611-39G= MANE Select | NP_002582.3:n.611-39G= |