Canonical Allele Identifier: CA1748625269

Genomic Alleles

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

Transcript Alleles

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