HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114147C>A , CM000667.2:g.140114147C>A | GRCh38 |
NC_000005.9:g.139493732C>A , CM000667.1:g.139493732C>A | GRCh37 |
NC_000005.8:g.139473916C>A | NCBI36 |
NG_041813.1:g.5025C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.-35C>A MANE Select | ENSP00000332706.3:n.-35C>A | |
ENST00000505703.2:c.-35C>A | ENSP00000498560.1:n.-35C>A | |
ENST00000651386.1:c.-35C>A | ENSP00000499133.1:n.-35C>A | |
ENST00000331327.4:c.-35C>A | ENSP00000332706.3:n.-35C>A | |
ENST00000502351.1:n.389C>A | ||
ENST00000505703.1:n.431C>A | ||
NM_005859.4:c.-35C>A | NP_005850.1:n.-35C>A | |
NM_005859.5:c.-35C>A MANE Select | NP_005850.1:n.-35C>A |