HGVS | Genome Assembly |
---|---|
NC_000016.10:g.74713435A>G , CM000678.2:g.74713435A>G | GRCh38 |
NC_000016.9:g.74747333A>G , CM000678.1:g.74747333A>G | GRCh37 |
NC_000016.8:g.73304834A>G | NCBI36 |
NG_017070.1:g.66397T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000219368.8:c.*755T>C MANE Select | ENSP00000219368.3:n.*755T>C | |
ENST00000219368.7:c.*755T>C | ENSP00000219368.3:n.*755T>C | |
ENST00000562145.1:n.1595T>C | ||
NM_024306.4:c.*755T>C | NP_077282.3:n.*755T>C | |
XM_011523319.1:c.*755T>C | XP_011521621.1:n.*755T>C | |
XM_011523319.2:c.*755T>C | XP_011521621.1:n.*755T>C | |
NM_024306.5:c.*755T>C MANE Select | NP_077282.3:n.*755T>C |