HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20242544C>G , CM000684.2:g.20242544C>G | GRCh38 |
NC_000022.10:g.20230067C>G , CM000684.1:g.20230067C>G | GRCh37 |
NC_000022.9:g.18610067C>G | NCBI36 |
NG_012176.1:g.30750G>C | |
NG_012176.2:g.30750G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000043402.8:c.589G>C MANE Select | ENSP00000043402.7:p.Ala197Pro | |
ENST00000043402.7:c.589G>C | ENSP00000043402.7:p.Ala197Pro | |
ENST00000416372.5:c.648G>C | ||
ENST00000425986.1:c.846G>C | ||
NM_023004.5:c.589G>C | NP_075380.1:p.Ala197Pro | |
NM_023004.6:c.589G>C MANE Select | NP_075380.1:p.Ala197Pro |