Linked Data
MyVariant Identifiers:
chr19:g.41351262G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40845357G>A , CM000681.2:g.40845357G>A | GRCh38 |
| NC_000019.9:g.41351262G>A , CM000681.1:g.41351262G>A | GRCh37 |
| NC_000019.8:g.46043102G>A | NCBI36 |
| NG_008377.1:g.10091C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301141.10:c.1098C>T MANE Select | ENSP00000301141.4:p.Ile366= | |
| ENST00000301141.9:c.1098C>T | ENSP00000301141.4:p.Ile366= | |
| ENST00000596719.5:n.949C>T | ||
| ENST00000601627.1:c.119+43942G>A | ||
| ENST00000610301.1:c.1098C>T | ENSP00000477899.1:p.Ile366= | |
| NM_000762.5:c.1098C>T | NP_000753.3:p.Ile366= | |
| NM_000762.6:c.1098C>T MANE Select | NP_000753.3:p.Ile366= |