HGVS | Genome Assembly |
---|---|
NC_000007.14:g.142753767_142753768delinsCT , CM000669.2:g.142753767_142753768delinsCT | GRCh38 |
NC_000007.13:g.142461618_142461619delinsCT , CM000669.1:g.142461618_142461619delinsCT | GRCh37 |
NC_000007.12:g.142141192_142141193delinsCT | NCBI36 |
NG_008307.3:g.9284_9285delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000610416.2:c.370+32581_370+32582delinsCT (TRBC1) | ENSP00000482915.1:n.370+32581_370+32582delinsCT | |
ENST00000612126.4:c.591+1200_591+1201delinsCT (PRSS1) | ENSP00000479959.1:n.591+1200_591+1201delinsCT | |
ENST00000633114.1:c.321+1873_321+1874delinsCT (PRSS2) | ENSP00000487822.1:n.321+1873_321+1874delinsCT | |
ENST00000634019.1:c.82+4976_82+4977delinsCT (PRSS2) | ENSP00000488594.1:n.82+4976_82+4977delinsCT |