HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31860476G>C , CM000668.2:g.31860476G>C | GRCh38 |
NC_000006.11:g.31828253G>C , CM000668.1:g.31828253G>C | GRCh37 |
NC_000006.10:g.31936232G>C | NCBI36 |
NG_008201.1:g.7457C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375631.5:c.761C>G MANE Select | ENSP00000364782.4:p.Pro254Arg | |
ENST00000677054.1:n.2004C>G | ||
ENST00000677512.1:n.869C>G | ||
ENST00000678869.1:n.1435C>G | ||
ENST00000375631.4:c.761C>G | ENSP00000364782.4:p.Pro254Arg | |
ENST00000480384.1:n.790C>G | ||
ENST00000491768.5:c.761C>G | ENSP00000433127.1:p.Pro254Arg | |
ENST00000495807.1:n.1895C>G | ||
NM_000434.3:c.761C>G | NP_000425.1:p.Pro254Arg | |
NM_000434.4:c.761C>G MANE Select | NP_000425.1:p.Pro254Arg |