Linked Data
MyVariant Identifiers:
chr19:g.616030G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.616030G>C , CM000681.2:g.616030G>C | GRCh38 |
| NC_000019.9:g.616030G>C , CM000681.1:g.616030G>C | GRCh37 |
| NC_000019.8:g.567030G>C | NCBI36 |
| NG_023049.1:g.22539C>G | |
| NG_052810.1:g.31138G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251287.3:c.2226G>C MANE Select | ENSP00000251287.1:p.Val742= | |
| ENST00000251287.2:c.2226G>C | ENSP00000251287.1:p.Val742= | |
| NM_001194.3:c.2226G>C | NP_001185.3:p.Val742= | |
| NM_001194.4:c.2226G>C MANE Select | NP_001185.3:p.Val742= |