HGVS | Genome Assembly |
---|---|
NC_000012.12:g.102840444A>G , CM000674.2:g.102840444A>G | GRCh38 |
NC_000012.11:g.103234222A>G , CM000674.1:g.103234222A>G | GRCh37 |
NC_000012.10:g.101758352A>G | NCBI36 |
NG_008690.1:g.82159T>C | |
NG_008690.2:g.122967T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000553106.6:c.1271T>C MANE Select | ENSP00000448059.1:p.Leu424Ser | |
ENST00000307000.7:c.1256T>C | ENSP00000303500.2:p.Leu419Ser | |
ENST00000551114.2:n.933T>C | ||
ENST00000553106.5:c.1271T>C | ENSP00000448059.1:p.Leu424Ser | |
ENST00000635477.1:c.375T>C | ||
ENST00000635528.1:n.786T>C | ||
NM_000277.1:c.1271T>C | NP_000268.1:p.Leu424Ser | |
XM_011538422.1:c.1214T>C | XP_011536724.1:p.Leu405Ser | |
NM_000277.2:c.1271T>C | NP_000268.1:p.Leu424Ser | |
NM_001354304.1:c.1271T>C | NP_001341233.1:p.Leu424Ser | |
NM_000277.3:c.1271T>C MANE Select | NP_000268.1:p.Leu424Ser | |
NM_001354304.2:c.1271T>C | NP_001341233.1:p.Leu424Ser |