Canonical Allele Identifier: CA10616973
Gene: PRSS12 HGNC NCBI

Linked Data

ClinVar Variation Id: 347376
ClinVar RCV Id: RCV000355037
dbSNP Id: rs886059025
gnomAD v3: 4-118281094-G-C
gnomAD v4: 4-118281094-G-C
MyVariant Identifiers: chr4:g.119202249G>C (hg19) chr4:g.118281094G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.118281094G>C , CM000666.2:g.118281094G>C GRCh38
NC_000004.11:g.119202249G>C , CM000666.1:g.119202249G>C GRCh37
NC_000004.10:g.119421697G>C NCBI36
NG_023350.1:g.76674C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296498.3:c.*842C>G MANE Select ENSP00000296498.3:n.*842C>G
NM_003619.3:c.*842C>G NP_003610.2:n.*842C>G
NM_003619.4:c.*842C>G MANE Select NP_003610.2:n.*842C>G
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