HGVS | Genome Assembly |
---|---|
NC_000014.9:g.22843357G>T , CM000676.2:g.22843357G>T | GRCh38 |
NC_000014.8:g.23312566G>T , CM000676.1:g.23312566G>T | GRCh37 |
NC_000014.7:g.22382406G>T | NCBI36 |
NG_046989.1:g.11825G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311852.11:c.789G>T MANE Select | ENSP00000308208.6:p.Trp263Cys | |
ENST00000548162.2:c.789G>T | ENSP00000506068.1:p.Trp263Cys | |
ENST00000680097.1:c.*104G>T | ENSP00000506631.1:n.*104G>T | |
ENST00000680941.1:c.*187G>T | ENSP00000506378.1:n.*187G>T | |
ENST00000311852.10:c.789G>T | ENSP00000308208.6:p.Trp263Cys | |
ENST00000548162.1:n.1031G>T | ||
NM_004995.3:c.789G>T | NP_004986.1:p.Trp263Cys | |
NM_004995.4:c.789G>T MANE Select | NP_004986.1:p.Trp263Cys |