HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136687439T>G , CM000671.2:g.136687439T>G | GRCh38 |
NC_000009.11:g.139581891T>G , CM000671.1:g.139581891T>G | GRCh37 |
NC_000009.10:g.138701712T>G | NCBI36 |
NG_008090.1:g.5021A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.-82A>C MANE Select | ENSP00000360761.2:n.-82A>C | |
NM_001012727.1:c.-82A>C | NP_001012745.1:n.-82A>C | |
NM_006412.3:c.-82A>C | NP_006403.2:n.-82A>C | |
NM_006412.4:c.-82A>C MANE Select | NP_006403.2:n.-82A>C | |
NM_001012727.2:c.-82A>C | NP_001012745.1:n.-82A>C |