Canonical Allele Identifier: CA350991904
Gene: PRSS56 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233388485C>A (hg19) chr2:g.232523775C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523775C>A , CM000664.2:g.232523775C>A GRCh38
NC_000002.11:g.233388485C>A , CM000664.1:g.233388485C>A GRCh37
NC_000002.10:g.233096729C>A NCBI36
NG_008028.1:g.2564C>A
NG_031969.1:g.8313C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1016C>A MANE Select ENSP00000479745.1:p.Ser339Tyr
ENST00000449534.6:c.1019C>A ENSP00000473410.1:p.Ser340Tyr
ENST00000617714.1:c.1016C>A ENSP00000479745.1:p.Ser339Tyr
NM_001195129.1:c.1016C>A NP_001182058.1:p.Ser339Tyr
NM_001195129.2:c.1016C>A MANE Select NP_001182058.1:p.Ser339Tyr
NM_001369848.1:c.1019C>A NP_001356777.1:p.Ser340Tyr
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