Canonical Allele Identifier: CA1108082123

Linked Data

dbSNP Id: rs1798919307

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753570A>G , CM000669.2:g.142753570A>G GRCh38
NC_000007.13:g.142461421A>G , CM000669.1:g.142461421A>G GRCh37
NC_000007.12:g.142140995A>G NCBI36
NG_008307.3:g.9087A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32384A>G (TRBC1) ENSP00000482915.1:n.370+32384A>G
ENST00000612126.4:c.591+1003A>G (PRSS1) ENSP00000479959.1:n.591+1003A>G
ENST00000633114.1:c.321+1676A>G (PRSS2) ENSP00000487822.1:n.321+1676A>G
ENST00000634019.1:c.82+4779A>G (PRSS2) ENSP00000488594.1:n.82+4779A>G