Linked Data
MyVariant Identifiers:
chr15:g.41223789C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40931591C>A , CM000677.2:g.40931591C>A | GRCh38 |
| NC_000015.9:g.41223789C>A , CM000677.1:g.41223789C>A | GRCh37 |
| NC_000015.8:g.39011081C>A | NCBI36 |
| NG_046974.1:g.7259C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249749.7:c.483C>A MANE Select | ENSP00000249749.5:p.Thr161= | |
| ENST00000249749.6:c.483C>A | ENSP00000249749.5:p.Thr161= | |
| ENST00000559440.1:n.712C>A | ||
| NM_019074.3:c.483C>A | NP_061947.1:p.Thr161= | |
| NM_019074.4:c.483C>A MANE Select | NP_061947.1:p.Thr161= |