HGVS | Genome Assembly |
---|---|
NC_000006.12:g.112069743A>C , CM000668.2:g.112069743A>C | GRCh38 |
NC_000006.11:g.112390946A>C , CM000668.1:g.112390946A>C | GRCh37 |
NC_000006.10:g.112497639A>C | NCBI36 |
NG_011748.1:g.20669A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361714.5:c.*123A>C | ENSP00000354734.2:n.*123A>C | |
ENST00000368666.6:c.*123A>C | ENSP00000357655.3:n.*123A>C |