Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372228C>G , CM000679.2:g.44372228C>G | GRCh38 |
| NC_000017.10:g.42449596C>G , CM000679.1:g.42449596C>G | GRCh37 |
| NC_000017.9:g.39805122C>G | NCBI36 |
| NG_008331.1:g.22278G>C , LRG_479:g.22278G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.*136G>C MANE Select | ENSP00000262407.5:n.*136G>C | |
| ENST00000648408.1:c.2570G>C | ||
| ENST00000262407.5:c.*136G>C | ENSP00000262407.5:n.*136G>C | |
| ENST00000587295.5:c.449G>C | ||
| ENST00000588098.1:c.233G>C | ||
| NM_000419.3:c.*136G>C , LRG_479t1:c.*136G>C | NP_000410.2:n.*136G>C | |
| XM_011524749.1:c.*136G>C | XP_011523051.1:n.*136G>C | |
| XM_011524750.1:c.*136G>C | XP_011523052.1:n.*136G>C | |
| NM_000419.4:c.*136G>C | NP_000410.2:n.*136G>C | |
| NM_000419.5:c.*136G>C MANE Select | NP_000410.2:n.*136G>C |