HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60645840T>C , CM000676.2:g.60645840T>C | GRCh38 |
NC_000014.8:g.61112558T>C , CM000676.1:g.61112558T>C | GRCh37 |
NC_000014.7:g.60182311T>C | NCBI36 |
NG_008231.1:g.8598A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000645694.3:c.*443A>G MANE Select | ENSP00000494686.1:n.*443A>G | |
ENST00000247182.6:c.*443A>G | ENSP00000247182.5:n.*443A>G | |
ENST00000553535.2:n.986A>G | ||
ENST00000554986.2:c.*443A>G | ENSP00000452700.2:n.*443A>G | |
ENST00000555955.3:n.1935A>G | ||
NM_005982.3:c.*443A>G | NP_005973.1:n.*443A>G | |
XM_017021602.2:c.*717A>G | XP_016877091.1:n.*717A>G | |
NM_005982.4:c.*443A>G MANE Select | NP_005973.1:n.*443A>G |