HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401153T>C , CM000663.2:g.17401153T>C | GRCh38 |
NC_000001.10:g.17727649T>C , CM000663.1:g.17727649T>C | GRCh37 |
NC_000001.9:g.17600236T>C | NCBI36 |
NG_032943.1:g.33908T>C | |
NG_032943.2:g.33908T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.1852-52T>C MANE Select | ENSP00000483125.1:n.1852-52T>C | |
NM_207421.4:c.1852-52T>C MANE Select | NP_997304.3:n.1852-52T>C |