Canonical Allele Identifier: CA1108082219

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753646T>G , CM000669.2:g.142753646T>G GRCh38
NC_000007.13:g.142461497T>G , CM000669.1:g.142461497T>G GRCh37
NC_000007.12:g.142141071T>G NCBI36
NG_008307.3:g.9163T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32460T>G (TRBC1) ENSP00000482915.1:n.370+32460T>G
ENST00000612126.4:c.591+1079T>G (PRSS1) ENSP00000479959.1:n.591+1079T>G
ENST00000633114.1:c.321+1752T>G (PRSS2) ENSP00000487822.1:n.321+1752T>G
ENST00000634019.1:c.82+4855T>G (PRSS2) ENSP00000488594.1:n.82+4855T>G