Canonical Allele Identifier: CA9022304
Gene: PRSS57 HGNC NCBI

Linked Data

dbSNP Id: rs755280959
ExAC: 19:694996 C / G
gnomAD v2: 19-694996-C-G
gnomAD v4: 19-694996-C-G
MyVariant Identifiers: chr19:g.694996C>G (hg19) chr19:g.694996C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.694996C>G , CM000681.2:g.694996C>G GRCh38
NC_000019.9:g.694996C>G , CM000681.1:g.694996C>G GRCh37
NC_000019.8:g.645996C>G NCBI36
NG_051189.1:g.5536G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.80-29G>C MANE Select ENSP00000327386.6:n.80-29G>C
ENST00000329267.8:c.80-29G>C ENSP00000327386.6:n.80-29G>C
ENST00000613411.4:c.80-26G>C ENSP00000482358.1:n.80-26G>C
NM_001308209.1:c.80-29G>C NP_001295138.1:n.80-29G>C
NM_214710.3:c.80-26G>C NP_999875.1:n.80-26G>C
NM_214710.4:c.80-26G>C NP_999875.1:n.80-26G>C
NM_001308209.2:c.80-29G>C MANE Select NP_001295138.2:n.80-29G>C
NM_214710.5:c.80-26G>C NP_999875.2:n.80-26G>C
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