Linked Data
MyVariant Identifiers:
chr19:g.7594490A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7529604A>T , CM000681.2:g.7529604A>T | GRCh38 |
| NC_000019.9:g.7594490A>T , CM000681.1:g.7594490A>T | GRCh37 |
| NC_000019.8:g.7500490A>T | NCBI36 |
| NG_013374.1:g.453A>T | |
| NG_015806.1:g.11995A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.1251A>T MANE Select | ENSP00000264079.5:p.Thr417= | |
| ENST00000264079.10:c.1251A>T | ENSP00000264079.5:p.Thr417= | |
| ENST00000394321.9:n.1566A>T | ||
| ENST00000594692.1:n.247A>T | ||
| ENST00000595860.5:n.434A>T | ||
| ENST00000599334.1:c.128A>T | ||
| NM_020533.2:c.1251A>T | NP_065394.1:p.Thr417= | |
| NM_020533.3:c.1251A>T MANE Select | NP_065394.1:p.Thr417= |