Canonical Allele Identifier: CA2701638355
Gene: PRSS56 HGNC NCBI

Linked Data

dbSNP Id: rs998098614
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523615C>G , CM000664.2:g.232523615C>G GRCh38
NC_000002.11:g.233388325C>G , CM000664.1:g.233388325C>G GRCh37
NC_000002.10:g.233096569C>G NCBI36
NG_008028.1:g.2404C>G
NG_031969.1:g.8153C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1012+37C>G MANE Select ENSP00000479745.1:n.1012+37C>G
ENST00000449534.6:c.1012+37C>G ENSP00000473410.1:n.1012+37C>G
ENST00000617714.1:c.1012+37C>G ENSP00000479745.1:n.1012+37C>G
NM_001195129.1:c.1012+37C>G NP_001182058.1:n.1012+37C>G
NM_001195129.2:c.1012+37C>G MANE Select NP_001182058.1:n.1012+37C>G
NM_001369848.1:c.1012+37C>G NP_001356777.1:n.1012+37C>G
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