HGVS | Genome Assembly |
---|---|
NC_000016.10:g.74713349C>T , CM000678.2:g.74713349C>T | GRCh38 |
NC_000016.9:g.74747247C>T , CM000678.1:g.74747247C>T | GRCh37 |
NC_000016.8:g.73304748C>T | NCBI36 |
NG_017070.1:g.66483G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000219368.8:c.*841G>A MANE Select | ENSP00000219368.3:n.*841G>A | |
ENST00000219368.7:c.*841G>A | ENSP00000219368.3:n.*841G>A | |
ENST00000562145.1:n.1681G>A | ||
NM_024306.4:c.*841G>A | NP_077282.3:n.*841G>A | |
XM_011523319.1:c.*841G>A | XP_011521621.1:n.*841G>A | |
XM_011523319.2:c.*841G>A | XP_011521621.1:n.*841G>A | |
NM_024306.5:c.*841G>A MANE Select | NP_077282.3:n.*841G>A |