HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7933958G>C , CM000681.2:g.7933958G>C | GRCh38 |
NC_000019.9:g.7998843G>C , CM000681.1:g.7998843G>C | GRCh37 |
NC_000019.8:g.7904843G>C | NCBI36 |
NG_051180.1:g.14866C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270538.8:c.589C>G MANE Select | ENSP00000270538.2:p.Gln197Glu | |
ENST00000270538.7:c.589C>G | ENSP00000270538.2:p.Gln197Glu | |
ENST00000595831.5:c.576C>G | ||
ENST00000595876.5:c.*277C>G | ENSP00000471596.1:n.*277C>G | |
ENST00000597926.1:c.493C>G | ENSP00000469389.1:p.Gln165Glu | |
ENST00000600748.5:n.574C>G | ||
NM_006351.3:c.589C>G | NP_006342.2:p.Gln197Glu | |
NM_006351.4:c.589C>G MANE Select | NP_006342.2:p.Gln197Glu |