Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110177852C>T , CM000675.2:g.110177852C>T | GRCh38 |
| NC_000013.10:g.110830199C>T , CM000675.1:g.110830199C>T | GRCh37 |
| NC_000013.9:g.109628200C>T | NCBI36 |
| NG_011544.2:g.134298G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001845.6:c.2706G>A MANE Select | NP_001836.3:p.Pro902= |
| ENST00000375820.10:c.2706G>A MANE Select | ENSP00000364979.4:p.Pro902= |
| NM_001845.5:c.2706G>A | NP_001836.3:p.Pro902= |
| ENST00000375820.8:c.2706G>A | ENSP00000364979.4:p.Pro902= |
| XM_011521048.1:c.2514G>A | XP_011519350.1:p.Pro838= |
| XM_011521048.2:c.2514G>A | XP_011519350.1:p.Pro838= |