HGVS | Genome Assembly |
---|---|
NC_000007.14:g.142753770_142753771delinsCT , CM000669.2:g.142753770_142753771delinsCT | GRCh38 |
NC_000007.13:g.142461621_142461622delinsCT , CM000669.1:g.142461621_142461622delinsCT | GRCh37 |
NC_000007.12:g.142141195_142141196delinsCT | NCBI36 |
NG_008307.3:g.9287_9288delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000610416.2:c.370+32584_370+32585delinsCT (TRBC1) | ENSP00000482915.1:n.370+32584_370+32585delinsCT | |
ENST00000612126.4:c.591+1203_591+1204delinsCT (PRSS1) | ENSP00000479959.1:n.591+1203_591+1204delinsCT | |
ENST00000633114.1:c.321+1876_321+1877delinsCT (PRSS2) | ENSP00000487822.1:n.321+1876_321+1877delinsCT | |
ENST00000634019.1:c.82+4979_82+4980delinsCT (PRSS2) | ENSP00000488594.1:n.82+4979_82+4980delinsCT |