Linked Data
MyVariant Identifiers:
chr19:g.49477901G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48974644G>A , CM000681.2:g.48974644G>A | GRCh38 |
| NC_000019.9:g.49477901G>A , CM000681.1:g.49477901G>A | GRCh37 |
| NC_000019.8:g.54169713G>A | NCBI36 |
| NG_012923.1:g.23710C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323798.8:c.1398C>T MANE Select | ENSP00000317904.3:p.Phe466= | |
| ENST00000263276.6:c.1206C>T | ENSP00000263276.6:p.Phe402= | |
| ENST00000323798.7:c.1398C>T | ENSP00000317904.3:p.Phe466= | |
| ENST00000472004.5:n.153C>T | ||
| ENST00000496048.1:n.305C>T | ||
| NM_001161587.1:c.1206C>T | NP_001155059.1:p.Phe402= | |
| NM_002103.4:c.1398C>T | NP_002094.2:p.Phe466= | |
| NR_027763.1:n.1457C>T | ||
| NM_002103.5:c.1398C>T MANE Select | NP_002094.2:p.Phe466= | |
| NM_001161587.2:c.1206C>T | NP_001155059.1:p.Phe402= | |
| NR_027763.2:n.1413C>T |