Canonical Allele Identifier: CA1108082216

Linked Data

dbSNP Id: rs1585993979

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753643A>C , CM000669.2:g.142753643A>C GRCh38
NC_000007.13:g.142461494A>C , CM000669.1:g.142461494A>C GRCh37
NC_000007.12:g.142141068A>C NCBI36
NG_008307.3:g.9160A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32457A>C (TRBC1) ENSP00000482915.1:n.370+32457A>C
ENST00000612126.4:c.591+1076A>C (PRSS1) ENSP00000479959.1:n.591+1076A>C
ENST00000633114.1:c.321+1749A>C (PRSS2) ENSP00000487822.1:n.321+1749A>C
ENST00000634019.1:c.82+4852A>C (PRSS2) ENSP00000488594.1:n.82+4852A>C