Linked Data
MyVariant Identifiers:
chr7:g.155604520A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155811826A>G , CM000669.2:g.155811826A>G | GRCh38 |
| NC_000007.13:g.155604520A>G , CM000669.1:g.155604520A>G | GRCh37 |
| NC_000007.12:g.155297281A>G | NCBI36 |
| NG_007504.2:g.5448T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297261.7:c.297T>C MANE Select | ENSP00000297261.2:p.Thr99= | |
| ENST00000297261.6:c.297T>C | ENSP00000297261.2:p.Thr99= | |
| NM_000193.2:c.297T>C | NP_000184.1:p.Thr99= | |
| NM_000193.3:c.297T>C | NP_000184.1:p.Thr99= | |
| NM_000193.4:c.297T>C MANE Select | NP_000184.1:p.Thr99= |