Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.49636677C>G , CM000681.2:g.49636677C>G | GRCh38 |
| NC_000019.9:g.50139934C>G , CM000681.1:g.50139934C>G | GRCh37 |
| NC_000019.8:g.54831746C>G | NCBI36 |
| NG_042222.1:g.8467G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000246792.4:c.395G>C MANE Select | ENSP00000246792.2:p.Arg132Pro | |
| ENST00000246792.3:c.395G>C | ENSP00000246792.2:p.Arg132Pro | |
| ENST00000601532.1:n.535G>C | ||
| NM_006270.3:c.395G>C | NP_006261.1:p.Arg132Pro | |
| NM_006270.4:c.395G>C | NP_006261.1:p.Arg132Pro | |
| NM_006270.5:c.395G>C MANE Select | NP_006261.1:p.Arg132Pro |