Linked Data
MyVariant Identifiers:
chr19:g.7593817C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7528931C>T , CM000681.2:g.7528931C>T | GRCh38 |
| NC_000019.9:g.7593817C>T , CM000681.1:g.7593817C>T | GRCh37 |
| NC_000019.8:g.7499817C>T | NCBI36 |
| NG_015806.1:g.11322C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264079.11:c.1095C>T MANE Select | ENSP00000264079.5:p.Thr365= | |
| ENST00000264079.10:c.1095C>T | ENSP00000264079.5:p.Thr365= | |
| ENST00000394321.9:n.1410C>T | ||
| ENST00000595860.5:n.278C>T | ||
| NM_020533.2:c.1095C>T | NP_065394.1:p.Thr365= | |
| NM_020533.3:c.1095C>T MANE Select | NP_065394.1:p.Thr365= |