HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136687412T>C , CM000671.2:g.136687412T>C | GRCh38 |
NC_000009.11:g.139581864T>C , CM000671.1:g.139581864T>C | GRCh37 |
NC_000009.10:g.138701685T>C | NCBI36 |
NG_008090.1:g.5048A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.-55A>G MANE Select | ENSP00000360761.2:n.-55A>G | |
ENST00000371696.6:c.-55A>G | ENSP00000360761.2:n.-55A>G | |
NM_001012727.1:c.-55A>G | NP_001012745.1:n.-55A>G | |
NM_006412.3:c.-55A>G | NP_006403.2:n.-55A>G | |
NM_006412.4:c.-55A>G MANE Select | NP_006403.2:n.-55A>G | |
NM_001012727.2:c.-55A>G | NP_001012745.1:n.-55A>G |