Canonical Allele Identifier: CA1108082810

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753951T>G , CM000669.2:g.142753951T>G GRCh38
NC_000007.13:g.142461802T>G , CM000669.1:g.142461802T>G GRCh37
NC_000007.12:g.142141376T>G NCBI36
NG_008307.3:g.9468T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32765T>G (TRBC1) ENSP00000482915.1:n.370+32765T>G
ENST00000612126.4:c.591+1384T>G (PRSS1) ENSP00000479959.1:n.591+1384T>G
ENST00000633114.1:c.321+2057T>G (PRSS2) ENSP00000487822.1:n.321+2057T>G
ENST00000634019.1:c.82+5160T>G (PRSS2) ENSP00000488594.1:n.82+5160T>G