HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154904985G>C , CM000685.2:g.154904985G>C | GRCh38 |
NC_000023.10:g.154133260G>C , CM000685.1:g.154133260G>C | GRCh37 |
NC_000023.9:g.153786454G>C | NCBI36 |
NG_011403.1:g.122739C>G | |
NG_011403.2:g.122739C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5412C>G MANE Select | ENSP00000353393.4:p.Phe1804Leu | |
ENST00000360256.8:c.5412C>G | ENSP00000353393.4:p.Phe1804Leu | |
NM_000132.3:c.5412C>G | NP_000123.1:p.Phe1804Leu | |
XM_011531126.1:c.5307C>G | XP_011529428.1:p.Phe1769Leu | |
NM_000132.4:c.5412C>G MANE Select | NP_000123.1:p.Phe1804Leu |