Canonical Allele Identifier: CA66948891
Gene: PRSS56 HGNC NCBI

Linked Data

dbSNP Id: rs978703768

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523548T>G , CM000664.2:g.232523548T>G GRCh38
NC_000002.11:g.233388258T>G , CM000664.1:g.233388258T>G GRCh37
NC_000002.10:g.233096502T>G NCBI36
NG_008028.1:g.2337T>G
NG_031969.1:g.8086T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.982T>G MANE Select ENSP00000479745.1:p.Phe328Val
ENST00000449534.6:c.982T>G ENSP00000473410.1:p.Phe328Val
ENST00000617714.1:c.982T>G ENSP00000479745.1:p.Phe328Val
NM_001195129.1:c.982T>G NP_001182058.1:p.Phe328Val
NM_001195129.2:c.982T>G MANE Select NP_001182058.1:p.Phe328Val
NM_001369848.1:c.982T>G NP_001356777.1:p.Phe328Val