HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586452T= , CM000673.2:g.67586452T= | GRCh38 |
NC_000011.9:g.67353923T= , CM000673.1:g.67353923T= | GRCh37 |
NC_000011.8:g.67110499T= | NCBI36 |
NG_012075.1:g.7858T= , LRG_723:g.7858T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.400T= | ENSP00000381604.1:p.Cys134= | |
ENST00000398606.10:c.508T= MANE Select | ENSP00000381607.3:p.Cys170= | |
ENST00000646888.1:c.*224T= | ENSP00000494477.1:n.*224T= | |
ENST00000398603.5:c.400T= | ENSP00000381604.1:p.Cys134= | |
ENST00000398606.7:c.508T= | ENSP00000381607.3:p.Cys170= | |
ENST00000467591.1:n.619T= | ||
ENST00000494593.1:n.1480T= | ||
ENST00000498765.5:c.571T= | ||
NM_000852.3:c.508T= , LRG_723t1:c.508T= | NP_000843.1:p.Cys170= | |
NM_000852.4:c.508T= MANE Select | NP_000843.1:p.Cys170= |