Canonical Allele Identifier: CA1108082486

Linked Data

dbSNP Id: rs1811090

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753685G>T , CM000669.2:g.142753685G>T GRCh38
NG_008307.3:g.9202G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32499G>T (TRBC1) ENSP00000482915.1:n.370+32499G>T
ENST00000612126.4:c.591+1118G>T (PRSS1) ENSP00000479959.1:n.591+1118G>T
ENST00000633114.1:c.321+1791G>T (PRSS2) ENSP00000487822.1:n.321+1791G>T
ENST00000634019.1:c.82+4894G>T (PRSS2) ENSP00000488594.1:n.82+4894G>T