Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624399G>C , CM000679.2:g.41624399G>C | GRCh38 |
| NC_000017.10:g.39780651G>C , CM000679.1:g.39780651G>C | GRCh37 |
| NC_000017.9:g.37034177G>C | NCBI36 |
| NG_008625.1:g.5232C>G | |
| NG_009090.2:g.167314C>G , LRG_401:g.167314C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.111C>G MANE Select | ENSP00000308452.8:p.Ala37= | |
| ENST00000311208.12:c.111C>G | ENSP00000308452.8:p.Ala37= | |
| ENST00000463128.5:c.-312-193C>G | ENSP00000468672.1:n.-312-193C>G | |
| ENST00000491673.1:n.177C>G | ||
| ENST00000540235.5:c.-95C>G | ENSP00000441751.2:n.-95C>G | |
| ENST00000577817.3:c.66C>G | ENSP00000467418.1:p.Ala22= | |
| NM_000422.2:c.111C>G | NP_000413.1:p.Ala37= | |
| NM_000422.3:c.111C>G MANE Select | NP_000413.1:p.Ala37= |