Canonical Allele Identifier: CA12919742
Gene: PRSS51 HGNC NCBI

Linked Data

dbSNP Id: rs4281086
gnomAD v2: 8-10352308-C-A
gnomAD v3: 8-10494798-C-A
gnomAD v4: 8-10494798-C-A

Genomic Alleles

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

Transcript Alleles

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