HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586502C= , CM000673.2:g.67586502C= | GRCh38 |
NC_000011.9:g.67353973C= , CM000673.1:g.67353973C= | GRCh37 |
NC_000011.8:g.67110549C= | NCBI36 |
NG_012075.1:g.7908C= , LRG_723:g.7908C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.450C= | ENSP00000381604.1:p.Ala150= | |
ENST00000398606.10:c.558C= MANE Select | ENSP00000381607.3:p.Ala186= | |
ENST00000646888.1:c.*274C= | ENSP00000494477.1:n.*274C= | |
ENST00000398603.5:c.450C= | ENSP00000381604.1:p.Ala150= | |
ENST00000398606.7:c.558C= | ENSP00000381607.3:p.Ala186= | |
ENST00000467591.1:n.669C= | ||
ENST00000494593.1:n.1530C= | ||
ENST00000498765.5:c.621C= | ||
NM_000852.3:c.558C= , LRG_723t1:c.558C= | NP_000843.1:p.Ala186= | |
NM_000852.4:c.558C= MANE Select | NP_000843.1:p.Ala186= |