Linked Data
MyVariant Identifiers:
chr6:g.3225726G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225492G>C , CM000668.2:g.3225492G>C | GRCh38 |
| NC_000006.11:g.3225726G>C , CM000668.1:g.3225726G>C | GRCh37 |
| NC_000006.10:g.3170725G>C | NCBI36 |
| NG_016715.1:g.7243C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.597C>G MANE Select | ENSP00000259818.6:p.Thr199= | |
| ENST00000680070.1:n.1527C>G | ||
| ENST00000681707.1:n.1424C>G | ||
| ENST00000681757.1:n.902C>G | ||
| ENST00000259818.7:c.597C>G | ENSP00000259818.6:p.Thr199= | |
| ENST00000473006.1:n.714C>G | ||
| NM_178012.4:c.597C>G | NP_821080.1:p.Thr199= | |
| XM_011514571.1:c.381C>G | XP_011512873.1:p.Thr127= | |
| NM_178012.5:c.597C>G MANE Select | NP_821080.1:p.Thr199= |