Canonical Allele Identifier: CA1748625306

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753797A= , CM000669.2:g.142753797A= GRCh38
NC_000007.13:g.142461648A= , CM000669.1:g.142461648A= GRCh37
NC_000007.12:g.142141222A= NCBI36
NG_008307.3:g.9314A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32611A= (TRBC1) ENSP00000482915.1:n.370+32611A=
ENST00000612126.4:c.591+1230A= (PRSS1) ENSP00000479959.1:n.591+1230A=
ENST00000633114.1:c.321+1903A= (PRSS2) ENSP00000487822.1:n.321+1903A=
ENST00000634019.1:c.82+5006A= (PRSS2) ENSP00000488594.1:n.82+5006A=