Linked Data
MyVariant Identifiers:
chr2:g.29294908G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29072042G>T , CM000664.2:g.29072042G>T | GRCh38 |
| NC_000002.11:g.29294908G>T , CM000664.1:g.29294908G>T | GRCh37 |
| NC_000002.10:g.29148412G>T | NCBI36 |
| NG_021427.1:g.7220C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331664.6:c.2220C>A MANE Select | ENSP00000332809.4:p.Pro740= | |
| ENST00000331664.5:c.2220C>A | ENSP00000332809.4:p.Pro740= | |
| NM_001029883.2:c.2220C>A | NP_001025054.1:p.Pro740= | |
| XM_011532826.1:c.2220C>A | XP_011531128.1:p.Pro740= | |
| XR_939901.1:n.185+2875G>T | ||
| XR_939902.1:n.173+2887G>T | ||
| NM_001029883.3:c.2220C>A MANE Select | NP_001025054.1:p.Pro740= |