Canonical Allele Identifier: CA66948884
Gene: PRSS56 HGNC NCBI

Linked Data

dbSNP Id: rs866637365

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523542G>A , CM000664.2:g.232523542G>A GRCh38
NC_000002.11:g.233388252G>A , CM000664.1:g.233388252G>A GRCh37
NC_000002.10:g.233096496G>A NCBI36
NG_008028.1:g.2331G>A
NG_031969.1:g.8080G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.976G>A MANE Select ENSP00000479745.1:p.Ala326Thr
ENST00000449534.6:c.976G>A ENSP00000473410.1:p.Ala326Thr
ENST00000617714.1:c.976G>A ENSP00000479745.1:p.Ala326Thr
NM_001195129.1:c.976G>A NP_001182058.1:p.Ala326Thr
NM_001195129.2:c.976G>A MANE Select NP_001182058.1:p.Ala326Thr
NM_001369848.1:c.976G>A NP_001356777.1:p.Ala326Thr