HGVS | Genome Assembly |
---|---|
NC_000007.14:g.142753658_142753659insT , CM000669.2:g.142753658_142753659insT | GRCh38 |
NC_000007.13:g.142461509_142461510insT , CM000669.1:g.142461509_142461510insT | GRCh37 |
NC_000007.12:g.142141083_142141084insT | NCBI36 |
NG_008307.3:g.9175_9176insT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000610416.2:c.370+32472_370+32473insT (TRBC1) | ENSP00000482915.1:n.370+32472_370+32473insT | |
ENST00000612126.4:c.591+1091_591+1092insT (PRSS1) | ENSP00000479959.1:n.591+1091_591+1092insT | |
ENST00000633114.1:c.321+1764_321+1765insT (PRSS2) | ENSP00000487822.1:n.321+1764_321+1765insT | |
ENST00000634019.1:c.82+4867_82+4868insT (PRSS2) | ENSP00000488594.1:n.82+4867_82+4868insT |