Canonical Allele Identifier: CA1748625278

Linked Data

dbSNP Id: rs1225676026

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753754C>T , CM000669.2:g.142753754C>T GRCh38
NC_000007.13:g.142461605C>T , CM000669.1:g.142461605C>T GRCh37
NC_000007.12:g.142141179C>T NCBI36
NG_008307.3:g.9271C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32568C>T (TRBC1) ENSP00000482915.1:n.370+32568C>T
ENST00000612126.4:c.591+1187C>T (PRSS1) ENSP00000479959.1:n.591+1187C>T
ENST00000633114.1:c.321+1860C>T (PRSS2) ENSP00000487822.1:n.321+1860C>T
ENST00000634019.1:c.82+4963C>T (PRSS2) ENSP00000488594.1:n.82+4963C>T