HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225669C>G , CM000668.2:g.3225669C>G | GRCh38 |
NC_000006.11:g.3225903C>G , CM000668.1:g.3225903C>G | GRCh37 |
NC_000006.10:g.3170902C>G | NCBI36 |
NG_016715.1:g.7066G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.420G>C MANE Select | ENSP00000259818.6:p.Gly140= | |
ENST00000680070.1:n.1350G>C | ||
ENST00000681707.1:n.1247G>C | ||
ENST00000681757.1:n.725G>C | ||
ENST00000259818.7:c.420G>C | ENSP00000259818.6:p.Gly140= | |
ENST00000473006.1:n.537G>C | ||
NM_178012.4:c.420G>C | NP_821080.1:p.Gly140= | |
XM_011514571.1:c.204G>C | XP_011512873.1:p.Gly68= | |
NM_178012.5:c.420G>C MANE Select | NP_821080.1:p.Gly140= |