HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69353351G>T , CM000674.2:g.69353351G>T | GRCh38 |
NC_000012.11:g.69747131G>T , CM000674.1:g.69747131G>T | GRCh37 |
NC_000012.10:g.68033398G>T | NCBI36 |
NG_008195.1:g.9998G>T , LRG_768:g.9998G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.*132G>T MANE Select | ENSP00000261267.2:n.*132G>T | |
ENST00000261267.6:c.*132G>T | ENSP00000261267.2:n.*132G>T | |
ENST00000549690.1:c.*86G>T | ENSP00000449898.1:n.*86G>T | |
NM_000239.2:c.*132G>T , LRG_768t1:c.*132G>T | NP_000230.1:n.*132G>T | |
NM_000239.3:c.*132G>T MANE Select | NP_000230.1:n.*132G>T |