HGVS | Genome Assembly |
---|---|
NC_000007.14:g.142753774C>G , CM000669.2:g.142753774C>G | GRCh38 |
NC_000007.13:g.142461625C>G , CM000669.1:g.142461625C>G | GRCh37 |
NC_000007.12:g.142141199C>G | NCBI36 |
NG_008307.3:g.9291C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000610416.2:c.370+32588C>G (TRBC1) | ENSP00000482915.1:n.370+32588C>G | |
ENST00000612126.4:c.591+1207C>G (PRSS1) | ENSP00000479959.1:n.591+1207C>G | |
ENST00000633114.1:c.321+1880C>G (PRSS2) | ENSP00000487822.1:n.321+1880C>G | |
ENST00000634019.1:c.82+4983C>G (PRSS2) | ENSP00000488594.1:n.82+4983C>G |