Canonical Allele Identifier: CA66948895
Gene: PRSS56 HGNC NCBI

Linked Data

dbSNP Id: rs12617886

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523555A>C , CM000664.2:g.232523555A>C GRCh38
NC_000002.11:g.233388265A>C , CM000664.1:g.233388265A>C GRCh37
NC_000002.10:g.233096509A>C NCBI36
NG_008028.1:g.2344A>C
NG_031969.1:g.8093A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.989A>C MANE Select ENSP00000479745.1:p.Asp330Ala
ENST00000449534.6:c.989A>C ENSP00000473410.1:p.Asp330Ala
ENST00000617714.1:c.989A>C ENSP00000479745.1:p.Asp330Ala
NM_001195129.1:c.989A>C NP_001182058.1:p.Asp330Ala
NM_001195129.2:c.989A>C MANE Select NP_001182058.1:p.Asp330Ala
NM_001369848.1:c.989A>C NP_001356777.1:p.Asp330Ala