HGVS | Genome Assembly |
---|---|
NC_000002.12:g.25161603G>A , CM000664.2:g.25161603G>A | GRCh38 |
NC_000002.11:g.25384472G>A , CM000664.1:g.25384472G>A | GRCh37 |
NC_000002.10:g.25237976G>A | NCBI36 |
NG_008997.1:g.12088C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395826.7:c.282C>T MANE Select | ENSP00000379170.2:p.Ser94= | |
ENST00000264708.7:c.282C>T | ENSP00000264708.3:p.Ser94= | |
ENST00000380794.5:c.282C>T | ENSP00000370171.1:p.Ser94= | |
ENST00000395826.6:c.282C>T | ENSP00000379170.2:p.Ser94= | |
ENST00000405623.5:c.282C>T | ENSP00000384092.1:p.Ser94= | |
ENST00000449220.1:c.282C>T | ENSP00000387993.1:p.Ser94= | |
NM_000939.2:c.282C>T | NP_000930.1:p.Ser94= | |
NM_001035256.1:c.282C>T | NP_001030333.1:p.Ser94= | |
XM_011532917.1:c.282C>T | XP_011531219.1:p.Ser94= | |
NM_000939.3:c.282C>T | NP_000930.1:p.Ser94= | |
NM_001035256.2:c.282C>T | NP_001030333.1:p.Ser94= | |
NM_001319204.1:c.282C>T | NP_001306133.1:p.Ser94= | |
NM_001319205.1:c.282C>T | NP_001306134.1:p.Ser94= | |
NM_000939.4:c.282C>T MANE Select | NP_000930.1:p.Ser94= | |
NM_001319204.2:c.282C>T | NP_001306133.1:p.Ser94= | |
NM_001319205.2:c.282C>T | NP_001306134.1:p.Ser94= | |
NM_001035256.3:c.282C>T | NP_001030333.1:p.Ser94= |