HGVS | Genome Assembly |
---|---|
NC_000007.14:g.142753651T>C , CM000669.2:g.142753651T>C | GRCh38 |
NC_000007.13:g.142461502T>C , CM000669.1:g.142461502T>C | GRCh37 |
NC_000007.12:g.142141076T>C | NCBI36 |
NG_008307.3:g.9168T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000610416.2:c.370+32465T>C (TRBC1) | ENSP00000482915.1:n.370+32465T>C | |
ENST00000612126.4:c.591+1084T>C (PRSS1) | ENSP00000479959.1:n.591+1084T>C | |
ENST00000633114.1:c.321+1757T>C (PRSS2) | ENSP00000487822.1:n.321+1757T>C | |
ENST00000634019.1:c.82+4860T>C (PRSS2) | ENSP00000488594.1:n.82+4860T>C |