Linked Data
MyVariant Identifiers:
chr2:g.176983701A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176118973A>C , CM000664.2:g.176118973A>C | GRCh38 |
| NC_000002.11:g.176983701A>C , CM000664.1:g.176983701A>C | GRCh37 |
| NC_000002.10:g.176691947A>C | NCBI36 |
| NG_008133.2:g.12210A>C , LRG_246:g.12210A>C | |
| NG_009225.1:g.1289A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249501.5:c.765A>C MANE Select | ENSP00000249501.4:p.Thr255= | |
| ENST00000249501.4:c.765A>C | ENSP00000249501.4:p.Thr255= | |
| ENST00000490088.2:n.589A>C | ||
| ENST00000549469.1:n.636A>C | ||
| NM_002148.3:c.765A>C , LRG_246t1:c.765A>C | NP_002139.2:p.Thr255= | |
| NM_002148.4:c.765A>C MANE Select | NP_002139.2:p.Thr255= |