Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47377049T>C , CM000664.2:g.47377049T>C | GRCh38 |
| NC_000002.11:g.47604188T>C , CM000664.1:g.47604188T>C | GRCh37 |
| NC_000002.10:g.47457692T>C | NCBI36 |
| NG_012352.2:g.36887T>C , LRG_215:g.36887T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002354.3:c.527T>C MANE Select | NP_002345.2:p.Leu176Pro |
| ENST00000263735.9:c.527T>C MANE Select | ENSP00000263735.4:p.Leu176Pro |
| NM_002354.2:c.527T>C , LRG_215t1:c.527T>C | NP_002345.2:p.Leu176Pro |
| ENST00000263735.8:c.527T>C | ENSP00000263735.4:p.Leu176Pro |
| ENST00000405271.5:c.611T>C | ENSP00000385476.1:p.Leu204Pro |
| ENST00000456133.5:c.611T>C | ENSP00000410675.1:p.Leu204Pro |
| ENST00000490733.1:n.376T>C |