HGVS | Genome Assembly |
---|---|
NC_000009.12:g.69035750G>A , CM000671.2:g.69035750G>A | GRCh38 |
NC_000009.11:g.71650666G>A , CM000671.1:g.71650666G>A | GRCh37 |
NC_000009.10:g.70840486G>A | NCBI36 |
NG_008845.2:g.5188G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000642330.1:c.-33G>A | ENSP00000493770.1:n.-33G>A | |
ENST00000642889.1:c.-33G>A | ENSP00000493780.1:n.-33G>A | |
ENST00000643352.1:c.-33G>A | ENSP00000496488.1:n.-33G>A | |
ENST00000645088.1:c.-33G>A | ENSP00000495447.1:n.-33G>A | |
ENST00000377270.7:c.-33G>A | ENSP00000366482.3:n.-33G>A | |
ENST00000396364.7:c.-33G>A | ENSP00000379650.3:n.-33G>A | |
NM_000144.4:c.-33G>A | NP_000135.2:n.-33G>A | |
NM_001161706.1:c.-33G>A | NP_001155178.1:n.-33G>A | |
NM_181425.2:c.-33G>A | NP_852090.1:n.-33G>A |