HGVS | Genome Assembly |
---|---|
NC_000014.9:g.50910061C>A , CM000676.2:g.50910061C>A | GRCh38 |
NC_000014.8:g.51376779C>A , CM000676.1:g.51376779C>A | GRCh37 |
NC_000014.7:g.50446529C>A | NCBI36 |
NG_012796.1:g.39470G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216392.8:c.2011G>T MANE Select | ENSP00000216392.7:p.Gly671Cys | |
ENST00000216392.7:c.2011G>T | ENSP00000216392.7:p.Gly671Cys | |
ENST00000532107.2:n.184G>T | ||
ENST00000532462.5:c.2011G>T | ENSP00000431657.1:p.Gly671Cys | |
ENST00000544180.6:c.1909G>T | ENSP00000443787.1:p.Gly637Cys | |
NM_001163940.1:c.1909G>T | NP_001157412.1:p.Gly637Cys | |
NM_002863.4:c.2011G>T | NP_002854.3:p.Gly671Cys | |
NM_002863.5:c.2011G>T MANE Select | NP_002854.3:p.Gly671Cys | |
NM_001163940.2:c.1909G>T | NP_001157412.1:p.Gly637Cys |