Linked Data
MyVariant Identifiers:
chr17:g.27857463C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29530445C>G , CM000679.2:g.29530445C>G | GRCh38 |
| NC_000017.10:g.27857463C>G , CM000679.1:g.27857463C>G | GRCh37 |
| NC_000017.9:g.24881589C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261716.8:c.2187C>G MANE Select | ENSP00000261716.3:p.Thr729= | |
| ENST00000261716.7:c.2187C>G | ENSP00000261716.3:p.Thr729= | |
| ENST00000536202.1:c.1743C>G | ENSP00000438819.1:p.Thr581= | |
| ENST00000578653.1:n.271C>G | ||
| NM_020791.2:c.2187C>G | NP_065842.1:p.Thr729= | |
| NM_025142.1:c.1743C>G | NP_079418.1:p.Thr581= | |
| XM_011525060.1:c.2187C>G | XP_011523362.1:p.Thr729= | |
| XM_011525060.2:c.2187C>G | XP_011523362.1:p.Thr729= | |
| NM_020791.4:c.2187C>G MANE Select | NP_065842.1:p.Thr729= |