HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149927746G>C , CM000663.2:g.149927746G>C | GRCh38 |
NC_000001.10:g.149899638G>C , CM000663.1:g.149899638G>C | GRCh37 |
NC_000001.9:g.148166262G>C | NCBI36 |
NG_032777.1:g.5507C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.14C>G MANE Select | ENSP00000271628.8:p.Pro5Arg | |
ENST00000271628.8:c.14C>G | ENSP00000271628.8:p.Pro5Arg | |
NM_005850.4:c.14C>G | NP_005841.1:p.Pro5Arg | |
NM_005850.5:c.14C>G MANE Select | NP_005841.1:p.Pro5Arg |