HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67584763C= , CM000673.2:g.67584763C= | GRCh38 |
NC_000011.9:g.67352234C= , CM000673.1:g.67352234C= | GRCh37 |
NC_000011.8:g.67108810C= | NCBI36 |
NG_012075.1:g.6169C= , LRG_723:g.6169C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.223C= | ENSP00000381604.1:p.Arg75= | |
ENST00000398606.10:c.223C= MANE Select | ENSP00000381607.3:p.Arg75= | |
ENST00000646888.1:c.116C= | ENSP00000494477.1:p.Pro39= | |
ENST00000398603.5:c.223C= | ENSP00000381604.1:p.Arg75= | |
ENST00000398606.7:c.223C= | ENSP00000381607.3:p.Arg75= | |
ENST00000489040.1:n.222C= | ||
ENST00000494593.1:n.653C= | ||
ENST00000498765.5:c.186C= | ||
NM_000852.3:c.223C= , LRG_723t1:c.223C= | NP_000843.1:p.Arg75= | |
NM_000852.4:c.223C= MANE Select | NP_000843.1:p.Arg75= |