Canonical Allele Identifier: CA1748625413

Linked Data

dbSNP Id: rs1798939329

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753957C>T , CM000669.2:g.142753957C>T GRCh38
NC_000007.13:g.142461808C>T , CM000669.1:g.142461808C>T GRCh37
NC_000007.12:g.142141382C>T NCBI36
NG_008307.3:g.9474C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32771C>T (TRBC1) ENSP00000482915.1:n.370+32771C>T
ENST00000612126.4:c.591+1390C>T (PRSS1) ENSP00000479959.1:n.591+1390C>T
ENST00000633114.1:c.321+2063C>T (PRSS2) ENSP00000487822.1:n.321+2063C>T
ENST00000634019.1:c.82+5166C>T (PRSS2) ENSP00000488594.1:n.82+5166C>T