Linked Data
MyVariant Identifiers:
chr22:g.20230239G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20242716G>C , CM000684.2:g.20242716G>C | GRCh38 |
| NC_000022.10:g.20230239G>C , CM000684.1:g.20230239G>C | GRCh37 |
| NC_000022.9:g.18610239G>C | NCBI36 |
| NG_012176.1:g.30578C>G | |
| NG_012176.2:g.30578C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000043402.8:c.417C>G MANE Select | ENSP00000043402.7:p.Arg139= | |
| ENST00000043402.7:c.417C>G | ENSP00000043402.7:p.Arg139= | |
| ENST00000416372.5:c.476C>G | ||
| ENST00000425986.1:c.674C>G | ||
| ENST00000469601.1:n.553C>G | ||
| NM_023004.5:c.417C>G | NP_075380.1:p.Arg139= | |
| NM_023004.6:c.417C>G MANE Select | NP_075380.1:p.Arg139= |