Linked Data
MyVariant Identifiers:
chr22:g.38106493T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.37710486T>G , CM000684.2:g.37710486T>G | GRCh38 |
| NC_000022.10:g.38106493T>G , CM000684.1:g.38106493T>G | GRCh37 |
| NC_000022.9:g.36436439T>G | NCBI36 |
| NG_012857.1:g.18499T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644935.1:c.174T>G MANE Select | ENSP00000496394.1:p.Pro58= | |
| ENST00000344404.10:c.174T>G | ENSP00000340312.6:p.Pro58= | |
| ENST00000406386.7:c.174T>G | ENSP00000384312.3:p.Pro58= | |
| ENST00000455236.4:c.1131T>G | ENSP00000477208.1:n.1131T>G | |
| ENST00000492485.5:n.310T>G | ||
| NM_001039141.2:c.174T>G | NP_001034230.1:p.Pro58= | |
| NM_001039141.3:c.174T>G MANE Select | NP_001034230.1:p.Pro58= |