Canonical Allele Identifier: CA1763301064
Gene: PRSS51 HGNC NCBI

Linked Data

dbSNP Id: rs4281086

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10494798C>G , CM000670.2:g.10494798C>G GRCh38
NC_000008.10:g.10352308C>G , CM000670.1:g.10352308C>G GRCh37
NC_000008.9:g.10389718C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523024.2:c.343+2914G>C ENSP00000518528.1:n.343+2914G>C
ENST00000521149.2:n.203+3930G>C
ENST00000523024.1:n.609+2914G>C