Linked Data
MyVariant Identifiers:
chr2:g.219678890T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814167T>C , CM000664.2:g.218814167T>C | GRCh38 |
| NC_000002.11:g.219678890T>C , CM000664.1:g.219678890T>C | GRCh37 |
| NC_000002.10:g.219387134T>C | NCBI36 |
| NG_007959.1:g.37419T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.1164T>C MANE Select | ENSP00000258415.4:p.Ala388= | |
| ENST00000258415.8:c.1164T>C | ENSP00000258415.4:p.Ala388= | |
| ENST00000494263.5:n.1598T>C | ||
| NM_000784.3:c.1164T>C | NP_000775.1:p.Ala388= | |
| XM_017003488.2:c.744T>C | XP_016858977.1:p.Ala248= | |
| NM_000784.4:c.1164T>C MANE Select | NP_000775.1:p.Ala388= |