Canonical Allele Identifier: CA1108082579

Linked Data

dbSNP Id: rs1798928900

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753740C>T , CM000669.2:g.142753740C>T GRCh38
NC_000007.13:g.142461591C>T , CM000669.1:g.142461591C>T GRCh37
NC_000007.12:g.142141165C>T NCBI36
NG_008307.3:g.9257C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32554C>T (TRBC1) ENSP00000482915.1:n.370+32554C>T
ENST00000612126.4:c.591+1173C>T (PRSS1) ENSP00000479959.1:n.591+1173C>T
ENST00000633114.1:c.321+1846C>T (PRSS2) ENSP00000487822.1:n.321+1846C>T
ENST00000634019.1:c.82+4949C>T (PRSS2) ENSP00000488594.1:n.82+4949C>T