Canonical Allele Identifier: CA168152664
Gene: TRBC1 HGNC NCBI
PRSS1 HGNC NCBI
PRSS2 HGNC NCBI

Linked Data

dbSNP Id: rs907805888
gnomAD v3: 7-142753896-T-C
gnomAD v4: 7-142753896-T-C
MyVariant Identifiers: chr7:g.142461747T>C (hg19) chr7:g.142753896T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753896T>C , CM000669.2:g.142753896T>C GRCh38
NC_000007.13:g.142461747T>C , CM000669.1:g.142461747T>C GRCh37
NC_000007.12:g.142141321T>C NCBI36
NG_008307.3:g.9413T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32710T>C (TRBC1) ENSP00000482915.1:n.370+32710T>C
ENST00000612126.4:c.591+1329T>C (PRSS1) ENSP00000479959.1:n.591+1329T>C
ENST00000633114.1:c.321+2002T>C (PRSS2) ENSP00000487822.1:n.321+2002T>C
ENST00000634019.1:c.82+5105T>C (PRSS2) ENSP00000488594.1:n.82+5105T>C
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