HGVS | Genome Assembly |
---|---|
NC_000006.12:g.112069705G>C , CM000668.2:g.112069705G>C | GRCh38 |
NC_000006.11:g.112390908G>C , CM000668.1:g.112390908G>C | GRCh37 |
NC_000006.10:g.112497601G>C | NCBI36 |
NG_011748.1:g.20631G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361714.5:c.*85G>C | ENSP00000354734.2:n.*85G>C | |
ENST00000368666.6:c.*85G>C | ENSP00000357655.3:n.*85G>C |