Linked Data
MyVariant Identifiers:
chr17:g.39780588G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624336G>C , CM000679.2:g.41624336G>C | GRCh38 |
| NC_000017.10:g.39780588G>C , CM000679.1:g.39780588G>C | GRCh37 |
| NC_000017.9:g.37034114G>C | NCBI36 |
| NG_008625.1:g.5295C>G | |
| NG_009090.2:g.167377C>G , LRG_401:g.167377C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.174C>G MANE Select | ENSP00000308452.8:p.Ser58= | |
| ENST00000311208.12:c.174C>G | ENSP00000308452.8:p.Ser58= | |
| ENST00000463128.5:c.-312-130C>G | ENSP00000468672.1:n.-312-130C>G | |
| ENST00000491673.1:n.240C>G | ||
| ENST00000540235.5:c.-32C>G | ENSP00000441751.2:n.-32C>G | |
| ENST00000577817.3:c.129C>G | ENSP00000467418.1:p.Ser43= | |
| NM_000422.2:c.174C>G | NP_000413.1:p.Ser58= | |
| NM_000422.3:c.174C>G MANE Select | NP_000413.1:p.Ser58= |