HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586484T>C , CM000673.2:g.67586484T>C | GRCh38 |
NC_000011.9:g.67353955T>C , CM000673.1:g.67353955T>C | GRCh37 |
NC_000011.8:g.67110531T>C | NCBI36 |
NG_012075.1:g.7890T>C , LRG_723:g.7890T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.432T>C | ENSP00000381604.1:p.Tyr144= | |
ENST00000398606.10:c.540T>C MANE Select | ENSP00000381607.3:p.Tyr180= | |
ENST00000646888.1:c.*256T>C | ENSP00000494477.1:n.*256T>C | |
ENST00000398603.5:c.432T>C | ENSP00000381604.1:p.Tyr144= | |
ENST00000398606.7:c.540T>C | ENSP00000381607.3:p.Tyr180= | |
ENST00000467591.1:n.651T>C | ||
ENST00000494593.1:n.1512T>C | ||
ENST00000498765.5:c.603T>C | ||
NM_000852.3:c.540T>C , LRG_723t1:c.540T>C | NP_000843.1:p.Tyr180= | |
NM_000852.4:c.540T>C MANE Select | NP_000843.1:p.Tyr180= |