Canonical Allele Identifier: CA834446682
Gene: TRBC1 HGNC NCBI
PRSS1 HGNC NCBI
PRSS2 HGNC NCBI

Linked Data

dbSNP Id: rs1426711399
gnomAD v3: 7-142753780-C-T
gnomAD v4: 7-142753780-C-T
MyVariant Identifiers: chr7:g.142461631C>T (hg19) chr7:g.142753780C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753780C>T , CM000669.2:g.142753780C>T GRCh38
NC_000007.13:g.142461631C>T , CM000669.1:g.142461631C>T GRCh37
NC_000007.12:g.142141205C>T NCBI36
NG_008307.3:g.9297C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32594C>T (TRBC1) ENSP00000482915.1:n.370+32594C>T
ENST00000612126.4:c.591+1213C>T (PRSS1) ENSP00000479959.1:n.591+1213C>T
ENST00000633114.1:c.321+1886C>T (PRSS2) ENSP00000487822.1:n.321+1886C>T
ENST00000634019.1:c.82+4989C>T (PRSS2) ENSP00000488594.1:n.82+4989C>T
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