HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17393957T= , CM000663.2:g.17393957T= | GRCh38 |
NC_000001.10:g.17720453T= , CM000663.1:g.17720453T= | GRCh37 |
NC_000001.9:g.17593040T= | NCBI36 |
NG_032943.1:g.26712T= | |
NG_032943.2:g.26712T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000619609.1:c.1075-18T= MANE Select | ENSP00000483125.1:n.1075-18T= | |
NM_207421.4:c.1075-18T= MANE Select | NP_997304.3:n.1075-18T= |