HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586462C= , CM000673.2:g.67586462C= | GRCh38 |
NC_000011.9:g.67353933C= , CM000673.1:g.67353933C= | GRCh37 |
NC_000011.8:g.67110509C= | NCBI36 |
NG_012075.1:g.7868C= , LRG_723:g.7868C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.410C= | ENSP00000381604.1:p.Ala137= | |
ENST00000398606.10:c.518C= MANE Select | ENSP00000381607.3:p.Ala173= | |
ENST00000646888.1:c.*234C= | ENSP00000494477.1:n.*234C= | |
ENST00000398603.5:c.410C= | ENSP00000381604.1:p.Ala137= | |
ENST00000398606.7:c.518C= | ENSP00000381607.3:p.Ala173= | |
ENST00000467591.1:n.629C= | ||
ENST00000494593.1:n.1490C= | ||
ENST00000498765.5:c.581C= | ||
NM_000852.3:c.518C= , LRG_723t1:c.518C= | NP_000843.1:p.Ala173= | |
NM_000852.4:c.518C= MANE Select | NP_000843.1:p.Ala173= |