Canonical Allele Identifier: CA1108082702

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753927G>C , CM000669.2:g.142753927G>C GRCh38
NC_000007.13:g.142461778G>C , CM000669.1:g.142461778G>C GRCh37
NC_000007.12:g.142141352G>C NCBI36
NG_008307.3:g.9444G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32741G>C (TRBC1) ENSP00000482915.1:n.370+32741G>C
ENST00000612126.4:c.591+1360G>C (PRSS1) ENSP00000479959.1:n.591+1360G>C
ENST00000633114.1:c.321+2033G>C (PRSS2) ENSP00000487822.1:n.321+2033G>C
ENST00000634019.1:c.82+5136G>C (PRSS2) ENSP00000488594.1:n.82+5136G>C