HGVS | Genome Assembly |
---|---|
NC_000011.10:g.108147607T>C , CM000673.2:g.108147607T>C | GRCh38 |
NC_000011.9:g.108018334T>C , CM000673.1:g.108018334T>C | GRCh37 |
NC_000011.8:g.107523544T>C | NCBI36 |
NG_009888.1:g.31077T>C | |
NG_009888.2:g.35903T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265838.8:c.*217T>C | ENSP00000265838.4:n.*217T>C | |
NM_000019.3:c.*217T>C | NP_000010.1:n.*217T>C | |
XM_006718834.2:c.*217T>C | XP_006718897.1:n.*217T>C | |
XM_006718835.2:c.*217T>C | XP_006718898.1:n.*217T>C | |
XM_017017682.2:c.*217T>C | XP_016873171.1:n.*217T>C | |
XM_017017683.2:c.*217T>C | XP_016873172.1:n.*217T>C |