Canonical Allele Identifier: CA1748625393

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753938C= , CM000669.2:g.142753938C= GRCh38
NC_000007.13:g.142461789C= , CM000669.1:g.142461789C= GRCh37
NC_000007.12:g.142141363C= NCBI36
NG_008307.3:g.9455C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32752C= (TRBC1) ENSP00000482915.1:n.370+32752C=
ENST00000612126.4:c.591+1371C= (PRSS1) ENSP00000479959.1:n.591+1371C=
ENST00000633114.1:c.321+2044C= (PRSS2) ENSP00000487822.1:n.321+2044C=
ENST00000634019.1:c.82+5147C= (PRSS2) ENSP00000488594.1:n.82+5147C=