HGVS | Genome Assembly |
---|---|
NC_000016.10:g.177413C>A , CM000678.2:g.177413C>A | GRCh38 |
NC_000016.9:g.227412C>A , CM000678.1:g.227412C>A | GRCh37 |
NC_000016.8:g.167412C>A | NCBI36 |
NG_000006.1:g.38276C>A | |
NG_059186.1:g.5763C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320868.9:c.*2C>A MANE Select | ENSP00000322421.5:n.*2C>A | |
ENST00000397797.1:c.*2C>A | ENSP00000380899.1:n.*2C>A | |
ENST00000472694.1:n.567C>A | ||
NM_000558.4:c.*2C>A | NP_000549.1:n.*2C>A | |
NM_000558.5:c.*2C>A MANE Select | NP_000549.1:n.*2C>A |