Canonical Allele Identifier: CA1108082581

Linked Data

dbSNP Id: rs1798928995

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753741A>G , CM000669.2:g.142753741A>G GRCh38
NC_000007.13:g.142461592A>G , CM000669.1:g.142461592A>G GRCh37
NC_000007.12:g.142141166A>G NCBI36
NG_008307.3:g.9258A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32555A>G (TRBC1) ENSP00000482915.1:n.370+32555A>G
ENST00000612126.4:c.591+1174A>G (PRSS1) ENSP00000479959.1:n.591+1174A>G
ENST00000633114.1:c.321+1847A>G (PRSS2) ENSP00000487822.1:n.321+1847A>G
ENST00000634019.1:c.82+4950A>G (PRSS2) ENSP00000488594.1:n.82+4950A>G