HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20242630G>C , CM000684.2:g.20242630G>C | GRCh38 |
NC_000022.10:g.20230153G>C , CM000684.1:g.20230153G>C | GRCh37 |
NC_000022.9:g.18610153G>C | NCBI36 |
NG_012176.1:g.30664C>G | |
NG_012176.2:g.30664C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000043402.8:c.503C>G MANE Select | ENSP00000043402.7:p.Ala168Gly | |
ENST00000043402.7:c.503C>G | ENSP00000043402.7:p.Ala168Gly | |
ENST00000416372.5:c.562C>G | ||
ENST00000425986.1:c.760C>G | ||
ENST00000469601.1:n.639C>G | ||
NM_023004.5:c.503C>G | NP_075380.1:p.Ala168Gly | |
NM_023004.6:c.503C>G MANE Select | NP_075380.1:p.Ala168Gly |