Canonical Allele Identifier: CA834446670
Gene: TRBC1 HGNC NCBI
PRSS1 HGNC NCBI
PRSS2 HGNC NCBI

Linked Data

dbSNP Id: rs1396216001
gnomAD v3: 7-142753774-C-A
gnomAD v4: 7-142753774-C-A
MyVariant Identifiers: chr7:g.142461625C>A (hg19) chr7:g.142753774C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753774C>A , CM000669.2:g.142753774C>A GRCh38
NC_000007.13:g.142461625C>A , CM000669.1:g.142461625C>A GRCh37
NC_000007.12:g.142141199C>A NCBI36
NG_008307.3:g.9291C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32588C>A (TRBC1) ENSP00000482915.1:n.370+32588C>A
ENST00000612126.4:c.591+1207C>A (PRSS1) ENSP00000479959.1:n.591+1207C>A
ENST00000633114.1:c.321+1880C>A (PRSS2) ENSP00000487822.1:n.321+1880C>A
ENST00000634019.1:c.82+4983C>A (PRSS2) ENSP00000488594.1:n.82+4983C>A
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