Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.174729370G>T , CM000667.2:g.174729370G>T | GRCh38 |
| NC_000005.9:g.174156373G>T , CM000667.1:g.174156373G>T | GRCh37 |
| NC_000005.8:g.174088979G>T | NCBI36 |
| NG_008124.1:g.9799G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239243.7:c.591G>T MANE Select | ENSP00000239243.5:p.Ala197= | |
| ENST00000239243.6:c.591G>T | ENSP00000239243.5:p.Ala197= | |
| ENST00000507785.2:c.*215G>T | ENSP00000427425.1:n.*215G>T | |
| NM_002449.4:c.591G>T | NP_002440.2:p.Ala197= | |
| NM_001363626.1:c.*215G>T | NP_001350555.1:n.*215G>T | |
| NM_002449.5:c.591G>T MANE Select | NP_002440.2:p.Ala197= | |
| NM_001363626.2:c.*215G>T | NP_001350555.1:n.*215G>T |