HGVS | Genome Assembly |
---|---|
NC_000007.14:g.142753742C>G , CM000669.2:g.142753742C>G | GRCh38 |
NC_000007.13:g.142461593C>G , CM000669.1:g.142461593C>G | GRCh37 |
NC_000007.12:g.142141167C>G | NCBI36 |
NG_008307.3:g.9259C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000610416.2:c.370+32556C>G (TRBC1) | ENSP00000482915.1:n.370+32556C>G | |
ENST00000612126.4:c.591+1175C>G (PRSS1) | ENSP00000479959.1:n.591+1175C>G | |
ENST00000633114.1:c.321+1848C>G (PRSS2) | ENSP00000487822.1:n.321+1848C>G | |
ENST00000634019.1:c.82+4951C>G (PRSS2) | ENSP00000488594.1:n.82+4951C>G |