Canonical Allele Identifier: CA10619984
Gene: PRSS12 HGNC NCBI

Linked Data

ClinVar Variation Id: 347382
ClinVar RCV Id: RCV000385282
dbSNP Id: rs886059028
gnomAD v3: 4-118281405-G-T
gnomAD v4: 4-118281405-G-T
MyVariant Identifiers: chr4:g.119202560G>T (hg19) chr4:g.118281405G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.118281405G>T , CM000666.2:g.118281405G>T GRCh38
NC_000004.11:g.119202560G>T , CM000666.1:g.119202560G>T GRCh37
NC_000004.10:g.119422008G>T NCBI36
NG_023350.1:g.76363C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296498.3:c.*531C>A MANE Select ENSP00000296498.3:n.*531C>A
NM_003619.3:c.*531C>A NP_003610.2:n.*531C>A
NM_003619.4:c.*531C>A MANE Select NP_003610.2:n.*531C>A
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