Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.1270781G>C , CM000679.2:g.1270781G>C | GRCh38 |
| NC_000017.10:g.1174075G>C , CM000679.1:g.1174075G>C | GRCh37 |
| NC_000017.9:g.1120825G>C | NCBI36 |
| NG_042055.1:g.5218G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001164405.2:c.218G>C MANE Select | NP_001157877.1:p.Arg73Pro |
| ENST00000391429.2:c.218G>C MANE Select | ENSP00000375248.1:p.Arg73Pro |
| NM_001164405.1:c.218G>C | NP_001157877.1:p.Arg73Pro |
| ENST00000391429.1:c.218G>C | ENSP00000375248.1:p.Arg73Pro |