Canonical Allele Identifier: CA1748625198

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753647A= , CM000669.2:g.142753647A= GRCh38
NC_000007.13:g.142461498A= , CM000669.1:g.142461498A= GRCh37
NC_000007.12:g.142141072A= NCBI36
NG_008307.3:g.9164A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32461A= (TRBC1) ENSP00000482915.1:n.370+32461A=
ENST00000612126.4:c.591+1080A= (PRSS1) ENSP00000479959.1:n.591+1080A=
ENST00000633114.1:c.321+1753A= (PRSS2) ENSP00000487822.1:n.321+1753A=
ENST00000634019.1:c.82+4856A= (PRSS2) ENSP00000488594.1:n.82+4856A=