HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31861205G>C , CM000668.2:g.31861205G>C | GRCh38 |
NC_000006.11:g.31828982G>C , CM000668.1:g.31828982G>C | GRCh37 |
NC_000006.10:g.31936961G>C | NCBI36 |
NG_008201.1:g.6728C>G | |
NG_023058.1:g.22842C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375631.5:c.598C>G MANE Select | ENSP00000364782.4:p.Pro200Ala | |
ENST00000677054.1:n.1275C>G | ||
ENST00000677512.1:n.706C>G | ||
ENST00000678869.1:n.706C>G | ||
ENST00000375631.4:c.598C>G | ENSP00000364782.4:p.Pro200Ala | |
ENST00000480384.1:n.627C>G | ||
ENST00000491768.5:c.598C>G | ENSP00000433127.1:p.Pro200Ala | |
ENST00000495807.1:n.1166C>G | ||
NM_000434.3:c.598C>G | NP_000425.1:p.Pro200Ala | |
NM_000434.4:c.598C>G MANE Select | NP_000425.1:p.Pro200Ala |