HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31139561C= , CM000668.2:g.31139561C= | GRCh38 |
NC_000006.11:g.31107338C= , CM000668.1:g.31107338C= | GRCh37 |
NC_000006.10:g.31215317C= | NCBI36 |
NG_021348.1:g.29731C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259881.10:c.168-80C= MANE Select | ENSP00000259881.9:n.168-80C= | |
ENST00000259881.9:c.168-80C= | ENSP00000259881.9:n.168-80C= | |
ENST00000479581.5:n.62-80C= | ||
ENST00000481450.2:c.-22-80C= | ENSP00000447158.1:n.-22-80C= | |
ENST00000547221.1:c.24-80C= | ENSP00000449471.1:n.24-80C= | |
NM_014068.2:c.168-80C= | NP_054787.2:n.168-80C= | |
NM_014068.3:c.168-80C= MANE Select | NP_054787.2:n.168-80C= |