HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42184728A= , CM000679.2:g.42184728A= | GRCh38 |
NC_000017.10:g.40336746A= , CM000679.1:g.40336746A= | GRCh37 |
NC_000017.9:g.37590272A= | NCBI36 |
NG_011448.1:g.5725T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293330.1:c.22-200T= MANE Select | ENSP00000293330.1:n.22-200T= | |
NM_001524.1:c.22-200T= MANE Select | NP_001515.1:n.22-200T= |