HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134843185G>T , CM000671.2:g.134843185G>T | GRCh38 |
NC_000009.11:g.137735031G>T , CM000671.1:g.137735031G>T | GRCh37 |
NC_000009.10:g.136874852G>T | NCBI36 |
NG_008030.1:g.206380G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371820.4:c.*882G>T | ENSP00000360885.4:n.*882G>T | |
ENST00000371817.8:c.*882G>T MANE Select | ENSP00000360882.3:n.*882G>T | |
ENST00000371817.7:c.*882G>T | ENSP00000360882.3:n.*882G>T | |
ENST00000618395.4:c.*882G>T | ENSP00000481360.1:n.*882G>T | |
NM_000093.4:c.*882G>T | NP_000084.3:n.*882G>T | |
NM_001278074.1:c.*882G>T | NP_001265003.1:n.*882G>T | |
NR_103451.2:n.71-22976C>A | ||
NM_000093.5:c.*882G>T MANE Select | NP_000084.3:n.*882G>T |