Linked Data
MyVariant Identifiers:
chr2:g.136558195T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135800625T>C , CM000664.2:g.135800625T>C | GRCh38 |
| NC_000002.11:g.136558195T>C , CM000664.1:g.136558195T>C | GRCh37 |
| NC_000002.10:g.136274665T>C | NCBI36 |
| NG_008104.2:g.59545A>G , LRG_338:g.59545A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264162.7:c.4848A>G MANE Select | ENSP00000264162.2:p.Ala1616= | |
| ENST00000264162.6:c.4848A>G | ENSP00000264162.2:p.Ala1616= | |
| ENST00000452974.1:c.2960-2487A>G | ENSP00000391231.1:n.2960-2487A>G | |
| NM_002299.2:c.4848A>G , LRG_338t1:c.4848A>G | NP_002290.2:p.Ala1616= | |
| NM_002299.3:c.4848A>G | NP_002290.2:p.Ala1616= | |
| XM_017004088.2:c.4848A>G | XP_016859577.1:p.Ala1616= | |
| NM_002299.4:c.4848A>G MANE Select | NP_002290.2:p.Ala1616= |