Canonical Allele Identifier: CA10619991
Gene: PRSS12 HGNC NCBI

Linked Data

ClinVar Variation Id: 347386
ClinVar RCV Id: RCV000287306
dbSNP Id: rs886059031
MyVariant Identifiers: chr4:g.119202831G>A (hg19) chr4:g.118281676G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.118281676G>A , CM000666.2:g.118281676G>A GRCh38
NC_000004.11:g.119202831G>A , CM000666.1:g.119202831G>A GRCh37
NC_000004.10:g.119422279G>A NCBI36
NG_023350.1:g.76092C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296498.3:c.*260C>T MANE Select ENSP00000296498.3:n.*260C>T
NM_003619.3:c.*260C>T NP_003610.2:n.*260C>T
NM_003619.4:c.*260C>T MANE Select NP_003610.2:n.*260C>T
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