HGVS | Genome Assembly |
---|---|
NC_000001.11:g.192812202G>T , CM000663.2:g.192812202G>T | GRCh38 |
NC_000001.10:g.192781332G>T , CM000663.1:g.192781332G>T | GRCh37 |
NC_000001.9:g.191047955G>T | NCBI36 |
NG_012800.1:g.8164G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000235382.7:c.*606G>T MANE Select | ENSP00000235382.5:n.*606G>T | |
ENST00000235382.6:c.*606G>T | ENSP00000235382.5:n.*606G>T | |
NM_002923.3:c.*606G>T | NP_002914.1:n.*606G>T | |
NM_002923.4:c.*606G>T MANE Select | NP_002914.1:n.*606G>T |