HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73641050G>C , CM000664.2:g.73641050G>C | GRCh38 |
NC_000002.11:g.73868177G>C , CM000664.1:g.73868177G>C | GRCh37 |
NC_000002.10:g.73721685G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.579C>G MANE Select | ENSP00000272425.3:p.Phe193Leu | |
ENST00000272425.3:c.579C>G | ENSP00000272425.3:p.Phe193Leu | |
NM_003960.3:c.579C>G | NP_003951.3:p.Phe193Leu | |
NM_003960.4:c.579C>G MANE Select | NP_003951.3:p.Phe193Leu |