Canonical Allele Identifier: CA350991259
Gene: PRSS56 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233388229A>G (hg19) chr2:g.232523519A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523519A>G , CM000664.2:g.232523519A>G GRCh38
NC_000002.11:g.233388229A>G , CM000664.1:g.233388229A>G GRCh37
NC_000002.10:g.233096473A>G NCBI36
NG_008028.1:g.2308A>G
NG_031969.1:g.8057A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.953A>G MANE Select ENSP00000479745.1:p.Lys318Arg
ENST00000449534.6:c.953A>G ENSP00000473410.1:p.Lys318Arg
ENST00000617714.1:c.953A>G ENSP00000479745.1:p.Lys318Arg
NM_001195129.1:c.953A>G NP_001182058.1:p.Lys318Arg
NM_001195129.2:c.953A>G MANE Select NP_001182058.1:p.Lys318Arg
NM_001369848.1:c.953A>G NP_001356777.1:p.Lys318Arg
Search 100 bp 5'
Search 100 bp 3'