Linked Data
MyVariant Identifiers:
chr22:g.38129371C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.37733364C>G , CM000684.2:g.37733364C>G | GRCh38 |
| NC_000022.10:g.38129371C>G , CM000684.1:g.38129371C>G | GRCh37 |
| NC_000022.9:g.36459317C>G | NCBI36 |
| NG_012857.1:g.41377C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644935.1:c.4014C>G MANE Select | ENSP00000496394.1:p.Gly1338= | |
| ENST00000344404.10:c.*3497C>G | ENSP00000340312.6:n.*3497C>G | |
| ENST00000406386.7:c.4014C>G | ENSP00000384312.3:p.Gly1338= | |
| NM_001039141.2:c.4014C>G | NP_001034230.1:p.Gly1338= | |
| XM_011530646.1:c.512-3005G>C | XP_011528948.1:n.512-3005G>C | |
| NM_001039141.3:c.4014C>G MANE Select | NP_001034230.1:p.Gly1338= |