Linked Data
MyVariant Identifiers:
chr22:g.38106490A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.37710483A>T , CM000684.2:g.37710483A>T | GRCh38 |
| NC_000022.10:g.38106490A>T , CM000684.1:g.38106490A>T | GRCh37 |
| NC_000022.9:g.36436436A>T | NCBI36 |
| NG_012857.1:g.18496A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644935.1:c.171A>T MANE Select | ENSP00000496394.1:p.Pro57= | |
| ENST00000344404.10:c.171A>T | ENSP00000340312.6:p.Pro57= | |
| ENST00000406386.7:c.171A>T | ENSP00000384312.3:p.Pro57= | |
| ENST00000455236.4:c.1128A>T | ENSP00000477208.1:n.1128A>T | |
| ENST00000492485.5:n.307A>T | ||
| NM_001039141.2:c.171A>T | NP_001034230.1:p.Pro57= | |
| NM_001039141.3:c.171A>T MANE Select | NP_001034230.1:p.Pro57= |