Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44374720A>C , CM000679.2:g.44374720A>C | GRCh38 |
| NC_000017.10:g.42452088A>C , CM000679.1:g.42452088A>C | GRCh37 |
| NC_000017.9:g.39807614A>C | NCBI36 |
| NG_008331.1:g.19786T>G , LRG_479:g.19786T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.2882T>G MANE Select | ENSP00000262407.5:p.Phe961Cys | |
| ENST00000648408.1:c.2313T>G | ||
| ENST00000262407.5:c.2882T>G | ENSP00000262407.5:p.Phe961Cys | |
| ENST00000587295.5:c.253+1113T>G | ||
| ENST00000592462.5:n.2393T>G | ||
| NM_000419.3:c.2882T>G , LRG_479t1:c.2882T>G | NP_000410.2:p.Phe961Cys | |
| XM_011524749.1:c.2842-250T>G | XP_011523051.1:n.2842-250T>G | |
| XM_011524750.1:c.2882T>G | XP_011523052.1:p.Phe961Cys | |
| NM_000419.4:c.2882T>G | NP_000410.2:p.Phe961Cys | |
| NM_000419.5:c.2882T>G MANE Select | NP_000410.2:p.Phe961Cys |