Linked Data
MyVariant Identifiers:
chr7:g.97816239T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.98186927T>C , CM000669.2:g.98186927T>C | GRCh38 |
| NC_000007.13:g.97816239T>C , CM000669.1:g.97816239T>C | GRCh37 |
| NC_000007.12:g.97654175T>C | NCBI36 |
| NG_013375.1:g.85043T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297293.6:c.927T>C MANE Select | ENSP00000297293.5:p.Thr309= | |
| ENST00000297293.5:c.927T>C | ENSP00000297293.5:p.Thr309= | |
| NM_014916.3:c.927T>C | NP_055731.2:p.Thr309= | |
| XM_011515981.1:c.921T>C | XP_011514283.1:p.Thr307= | |
| XM_011515981.3:c.921T>C | XP_011514283.1:p.Thr307= | |
| NM_014916.4:c.927T>C MANE Select | NP_055731.2:p.Thr309= |