HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67585237A>G , CM000673.2:g.67585237A>G | GRCh38 |
NC_000011.9:g.67352708A>G , CM000673.1:g.67352708A>G | GRCh37 |
NC_000011.8:g.67109284A>G | NCBI36 |
NG_012075.1:g.6643A>G , LRG_723:g.6643A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398603.6:c.332A>G | ENSP00000381604.1:p.Asn111Ser | |
ENST00000398606.10:c.332A>G MANE Select | ENSP00000381607.3:p.Asn111Ser | |
ENST00000646888.1:c.*48A>G | ENSP00000494477.1:n.*48A>G | |
ENST00000398603.5:c.332A>G | ENSP00000381604.1:p.Asn111Ser | |
ENST00000398606.7:c.332A>G | ENSP00000381607.3:p.Asn111Ser | |
ENST00000467591.1:n.443A>G | ||
ENST00000494593.1:n.1127A>G | ||
ENST00000498765.5:c.395A>G | ||
NM_000852.3:c.332A>G , LRG_723t1:c.332A>G | NP_000843.1:p.Asn111Ser | |
NM_000852.4:c.332A>G MANE Select | NP_000843.1:p.Asn111Ser |