HGVS | Genome Assembly |
---|---|
NC_000001.11:g.225937424A= , CM000663.2:g.225937424A= | GRCh38 |
NC_000001.10:g.226125124A= , CM000663.1:g.226125124A= | GRCh37 |
NC_000001.9:g.224191747A= | NCBI36 |
NG_008118.1:g.8797T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000366820.10:c.*17T= MANE Select | ENSP00000355785.5:n.*17T= | |
ENST00000366820.9:c.*17T= | ENSP00000355785.5:n.*17T= | |
ENST00000420304.6:c.*17T= | ENSP00000388009.2:n.*17T= | |
ENST00000616737.1:c.1116T= | ENSP00000484300.1:p.His372= | |
NM_001172425.1:c.*17T= | NP_001165896.1:n.*17T= | |
NM_003240.3:c.*17T= | NP_003231.2:n.*17T= | |
NM_001172425.2:c.*17T= | NP_001165896.1:n.*17T= | |
NM_003240.4:c.*17T= | NP_003231.2:n.*17T= | |
NM_003240.5:c.*17T= MANE Select | NP_003231.2:n.*17T= | |
NM_001172425.3:c.*17T= | NP_001165896.1:n.*17T= |