HGVS | Genome Assembly |
---|---|
NC_000006.12:g.112069740T>A , CM000668.2:g.112069740T>A | GRCh38 |
NC_000006.11:g.112390943T>A , CM000668.1:g.112390943T>A | GRCh37 |
NC_000006.10:g.112497636T>A | NCBI36 |
NG_011748.1:g.20666T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361714.5:c.*120T>A | ENSP00000354734.2:n.*120T>A | |
ENST00000368666.6:c.*120T>A | ENSP00000357655.3:n.*120T>A |