HGVS | Genome Assembly |
---|---|
NC_000004.12:g.71785040A= , CM000666.2:g.71785040A= | GRCh38 |
NC_000004.11:g.72650757A= , CM000666.1:g.72650757A= | GRCh37 |
NC_000004.10:g.72869621A= | NCBI36 |
NG_012837.2:g.25481T= | |
NG_012837.3:g.25481T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000504199.5:c.22-986T= | ENSP00000421725.1:n.22-986T= | |
ENST00000506245.1:c.-37+880T= | ENSP00000426718.1:n.-37+880T= | |
NM_001204306.1:c.-36-986T= | NP_001191235.1:n.-36-986T= | |
NM_001204307.1:c.22-986T= | NP_001191236.1:n.22-986T= |