HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584024G>A , CM000679.2:g.41584024G>A | GRCh38 |
NC_000017.10:g.39740276G>A , CM000679.1:g.39740276G>A | GRCh37 |
NC_000017.9:g.36993802G>A | NCBI36 |
NG_008624.1:g.7872C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.766-103C>T MANE Select | ENSP00000167586.6:n.766-103C>T | |
ENST00000167586.6:c.766-103C>T | ENSP00000167586.6:n.766-103C>T | |
ENST00000476662.1:n.216-103C>T | ||
NM_000526.4:c.766-103C>T | NP_000517.2:n.766-103C>T | |
NM_000526.5:c.766-103C>T MANE Select | NP_000517.3:n.766-103C>T |