Linked Data
MyVariant Identifiers:
chr2:g.219647061G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218782338G>T , CM000664.2:g.218782338G>T | GRCh38 |
| NC_000002.11:g.219647061G>T , CM000664.1:g.219647061G>T | GRCh37 |
| NC_000002.10:g.219355305G>T | NCBI36 |
| NG_007959.1:g.5590G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.156G>T MANE Select | ENSP00000258415.4:p.Arg52= | |
| ENST00000258415.8:c.156G>T | ENSP00000258415.4:p.Arg52= | |
| ENST00000445971.1:c.156G>T | ENSP00000404945.1:p.Arg52= | |
| ENST00000466602.1:n.165G>T | ||
| ENST00000494263.5:n.590G>T | ||
| NM_000784.3:c.156G>T | NP_000775.1:p.Arg52= | |
| XM_017003488.2:c.-74G>T | XP_016858977.1:n.-74G>T | |
| NM_000784.4:c.156G>T MANE Select | NP_000775.1:p.Arg52= |