Canonical Allele Identifier: CA2663619735
Gene: PRSS56 HGNC NCBI

Linked Data

gnomAD v4: 2-232523686-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523686G>A , CM000664.2:g.232523686G>A GRCh38
NC_000002.11:g.233388396G>A , CM000664.1:g.233388396G>A GRCh37
NC_000002.10:g.233096640G>A NCBI36
NG_008028.1:g.2475G>A
NG_031969.1:g.8224G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1013-86G>A MANE Select ENSP00000479745.1:n.1013-86G>A
ENST00000449534.6:c.1013-83G>A ENSP00000473410.1:n.1013-83G>A
ENST00000617714.1:c.1013-86G>A ENSP00000479745.1:n.1013-86G>A
NM_001195129.1:c.1013-86G>A NP_001182058.1:n.1013-86G>A
NM_001195129.2:c.1013-86G>A MANE Select NP_001182058.1:n.1013-86G>A
NM_001369848.1:c.1013-83G>A NP_001356777.1:n.1013-83G>A
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