HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39965484C>T , CM000679.2:g.39965484C>T | GRCh38 |
NC_000017.10:g.38121737C>T , CM000679.1:g.38121737C>T | GRCh37 |
NC_000017.9:g.35375263C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301659.9:c.-5-199C>T MANE Select | ENSP00000301659.4:n.-5-199C>T | |
ENST00000635792.1:c.-5-199C>T | ENSP00000490739.1:n.-5-199C>T | |
ENST00000301659.8:c.-5-199C>T | ENSP00000301659.4:n.-5-199C>T | |
NM_178171.4:c.-5-199C>T | NP_835465.2:n.-5-199C>T | |
XM_017024502.2:c.-5-199C>T | XP_016879991.1:n.-5-199C>T | |
XM_017024503.1:c.-5-199C>T | XP_016879992.1:n.-5-199C>T | |
XM_017024504.2:c.-5-199C>T | XP_016879993.1:n.-5-199C>T | |
NM_178171.5:c.-5-199C>T MANE Select | NP_835465.2:n.-5-199C>T |