HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20425136G>A , CM000684.2:g.20425136G>A | GRCh38 |
NC_000022.10:g.20779426G>A , CM000684.1:g.20779426G>A | GRCh37 |
NC_000022.9:g.19109426G>A | NCBI36 |
NG_031868.2:g.17724C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622235.5:c.*239C>T MANE Select | ENSP00000477564.2:n.*239C>T | |
ENST00000615031.4:c.*239C>T | ENSP00000479389.1:n.*239C>T | |
ENST00000622235.4:c.*239C>T | ENSP00000477564.1:n.*239C>T | |
ENST00000623402.1:c.*239C>T | ENSP00000485276.1:n.*239C>T | |
NM_153334.6:c.*239C>T | NP_699165.3:n.*239C>T | |
NM_182895.4:c.*239C>T | NP_878315.2:n.*239C>T | |
NM_153334.7:c.*239C>T | NP_699165.3:n.*239C>T | |
NM_182895.5:c.*239C>T MANE Select | NP_878315.2:n.*239C>T |