Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29074159C>G , CM000664.2:g.29074159C>G | GRCh38 |
| NC_000002.11:g.29297025C>G , CM000664.1:g.29297025C>G | GRCh37 |
| NC_000002.10:g.29150529C>G | NCBI36 |
| NG_021427.1:g.5103G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001029883.3:c.103G>C MANE Select | NP_001025054.1:p.Gly35Arg |
| ENST00000331664.6:c.103G>C MANE Select | ENSP00000332809.4:p.Gly35Arg |
| NM_001029883.2:c.103G>C | NP_001025054.1:p.Gly35Arg |
| ENST00000331664.5:c.103G>C | ENSP00000332809.4:p.Gly35Arg |
| XM_011532826.1:c.103G>C | XP_011531128.1:p.Gly35Arg |
| XR_939901.1:n.185+4992C>G | |
| XR_939902.1:n.173+5004C>G |