Linked Data
MyVariant Identifiers:
chr2:g.219757900G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218893178G>C , CM000664.2:g.218893178G>C | GRCh38 |
| NC_000002.11:g.219757900G>C , CM000664.1:g.219757900G>C | GRCh37 |
| NC_000002.10:g.219466144G>C | NCBI36 |
| NG_012179.1:g.17646G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.1161G>C MANE Select | ENSP00000258411.3:p.Thr387= | |
| ENST00000258411.7:c.1161G>C | ENSP00000258411.3:p.Thr387= | |
| NM_025216.2:c.1161G>C | NP_079492.2:p.Thr387= | |
| XM_011511928.1:c.1110G>C | XP_011510230.1:p.Thr370= | |
| XM_011511929.1:c.1065G>C | XP_011510231.1:p.Thr355= | |
| XM_011511930.1:c.781G>C | XP_011510232.1:p.Ala261Pro | |
| XM_011511929.2:c.1065G>C | XP_011510231.1:p.Thr355= | |
| NM_025216.3:c.1161G>C MANE Select | NP_079492.2:p.Thr387= |