Linked Data
MyVariant Identifiers:
chr19:g.7594058C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7529172C>T , CM000681.2:g.7529172C>T | GRCh38 |
| NC_000019.9:g.7594058C>T , CM000681.1:g.7594058C>T | GRCh37 |
| NC_000019.8:g.7500058C>T | NCBI36 |
| NG_013374.1:g.21C>T | |
| NG_015806.1:g.11563C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.1206C>T MANE Select | ENSP00000264079.5:p.Ile402= | |
| ENST00000264079.10:c.1206C>T | ENSP00000264079.5:p.Ile402= | |
| ENST00000394321.9:n.1521C>T | ||
| ENST00000594692.1:n.202C>T | ||
| ENST00000595860.5:n.389C>T | ||
| ENST00000599334.1:c.83C>T | ||
| NM_020533.2:c.1206C>T | NP_065394.1:p.Ile402= | |
| NM_020533.3:c.1206C>T MANE Select | NP_065394.1:p.Ile402= |