Canonical Allele Identifier: CA1748625389

Linked Data

dbSNP Id: rs1798937677

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753925G>A , CM000669.2:g.142753925G>A GRCh38
NC_000007.13:g.142461776G>A , CM000669.1:g.142461776G>A GRCh37
NC_000007.12:g.142141350G>A NCBI36
NG_008307.3:g.9442G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32739G>A (TRBC1) ENSP00000482915.1:n.370+32739G>A
ENST00000612126.4:c.591+1358G>A (PRSS1) ENSP00000479959.1:n.591+1358G>A
ENST00000633114.1:c.321+2031G>A (PRSS2) ENSP00000487822.1:n.321+2031G>A
ENST00000634019.1:c.82+5134G>A (PRSS2) ENSP00000488594.1:n.82+5134G>A