HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136687437T>G , CM000671.2:g.136687437T>G | GRCh38 |
NC_000009.11:g.139581889T>G , CM000671.1:g.139581889T>G | GRCh37 |
NC_000009.10:g.138701710T>G | NCBI36 |
NG_008090.1:g.5023A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.-80A>C MANE Select | ENSP00000360761.2:n.-80A>C | |
NM_001012727.1:c.-80A>C | NP_001012745.1:n.-80A>C | |
NM_006412.3:c.-80A>C | NP_006403.2:n.-80A>C | |
NM_006412.4:c.-80A>C MANE Select | NP_006403.2:n.-80A>C | |
NM_001012727.2:c.-80A>C | NP_001012745.1:n.-80A>C |