Canonical Allele Identifier: CA1748625289

Linked Data

dbSNP Id: rs916191913

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753771T>A , CM000669.2:g.142753771T>A GRCh38
NC_000007.13:g.142461622T>A , CM000669.1:g.142461622T>A GRCh37
NC_000007.12:g.142141196T>A NCBI36
NG_008307.3:g.9288T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32585T>A (TRBC1) ENSP00000482915.1:n.370+32585T>A
ENST00000612126.4:c.591+1204T>A (PRSS1) ENSP00000479959.1:n.591+1204T>A
ENST00000633114.1:c.321+1877T>A (PRSS2) ENSP00000487822.1:n.321+1877T>A
ENST00000634019.1:c.82+4980T>A (PRSS2) ENSP00000488594.1:n.82+4980T>A