HGVS | Genome Assembly |
---|---|
NC_000007.14:g.142753881G= , CM000669.2:g.142753881G= | GRCh38 |
NC_000007.13:g.142461732G= , CM000669.1:g.142461732G= | GRCh37 |
NC_000007.12:g.142141306G= | NCBI36 |
NG_008307.3:g.9398G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610416.2:c.370+32695G= (TRBC1) | ENSP00000482915.1:n.370+32695G= | |
ENST00000612126.4:c.591+1314G= (PRSS1) | ENSP00000479959.1:n.591+1314G= | |
ENST00000633114.1:c.321+1987G= (PRSS2) | ENSP00000487822.1:n.321+1987G= | |
ENST00000634019.1:c.82+5090G= (PRSS2) | ENSP00000488594.1:n.82+5090G= |