Canonical Allele Identifier: CA884128013
Gene: PRSS57 HGNC NCBI

Linked Data

dbSNP Id: rs966460101
MyVariant Identifiers: chr19:g.695134G>T (hg19) chr19:g.695134G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.695134G>T , CM000681.2:g.695134G>T GRCh38
NC_000019.9:g.695134G>T , CM000681.1:g.695134G>T GRCh37
NC_000019.8:g.646134G>T NCBI36
NG_051189.1:g.5398C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.80-167C>A MANE Select ENSP00000327386.6:n.80-167C>A
ENST00000329267.8:c.80-167C>A ENSP00000327386.6:n.80-167C>A
ENST00000613411.4:c.80-164C>A ENSP00000482358.1:n.80-164C>A
NM_001308209.1:c.80-167C>A NP_001295138.1:n.80-167C>A
NM_214710.3:c.80-164C>A NP_999875.1:n.80-164C>A
NM_214710.4:c.80-164C>A NP_999875.1:n.80-164C>A
NM_001308209.2:c.80-167C>A MANE Select NP_001295138.2:n.80-167C>A
NM_214710.5:c.80-164C>A NP_999875.2:n.80-164C>A
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