HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114145G>A , CM000667.2:g.140114145G>A | GRCh38 |
NC_000005.9:g.139493730G>A , CM000667.1:g.139493730G>A | GRCh37 |
NC_000005.8:g.139473914G>A | NCBI36 |
NG_041813.1:g.5023G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.-37G>A MANE Select | ENSP00000332706.3:n.-37G>A | |
ENST00000505703.2:c.-37G>A | ENSP00000498560.1:n.-37G>A | |
ENST00000651386.1:c.-37G>A | ENSP00000499133.1:n.-37G>A | |
ENST00000331327.4:c.-37G>A | ENSP00000332706.3:n.-37G>A | |
ENST00000502351.1:n.387G>A | ||
ENST00000505703.1:n.429G>A | ||
NM_005859.4:c.-37G>A | NP_005850.1:n.-37G>A | |
NM_005859.5:c.-37G>A MANE Select | NP_005850.1:n.-37G>A |