Canonical Allele Identifier: CA431803164
Gene: PRSS56 HGNC NCBI

Linked Data

gnomAD v4: 2-232523457-C-A
MyVariant Identifiers: chr2:g.233388167C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523457C>A , CM000664.2:g.232523457C>A GRCh38
NC_000002.11:g.233388167C>A , CM000664.1:g.233388167C>A GRCh37
NC_000002.10:g.233096411C>A NCBI36
NG_008028.1:g.2246C>A
NG_031969.1:g.7995C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.891C>A MANE Select ENSP00000479745.1:p.Pro297=
ENST00000449534.6:c.891C>A ENSP00000473410.1:p.Pro297=
ENST00000617714.1:c.891C>A ENSP00000479745.1:p.Pro297=
NM_001195129.1:c.891C>A NP_001182058.1:p.Pro297=
NM_001195129.2:c.891C>A MANE Select NP_001182058.1:p.Pro297=
NM_001369848.1:c.891C>A NP_001356777.1:p.Pro297=
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