Canonical Allele Identifier: CA225604314
Gene: PRSS23 HGNC NCBI
COSMIC:
COSN16530740 (not active)
MyVariant.info:
GRCh38 chr11:g.86792095C>A
GRCh37 chr11:g.86503137C>A
gnomAD v2:
11:86503137 C / A
gnomAD v3:
11:86792095 C / A
gnomAD v4:
chr11-86792095-C-A
Joint Max Group AF 0.08426905 (AMR)
Genomes Max Group AF 0.08426905 (AMR)
dbSNP:
2015747
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86792095C>A , CM000673.2:g.86792095C>A GRCh38
NC_000011.9:g.86503137C>A , CM000673.1:g.86503137C>A GRCh37
NC_000011.8:g.86180785C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000527521.1:c.-14+900C>A ENSP00000435951.1:n.-14+900C>A
NM_001293180.1:c.-14+900C>A NP_001280109.1:n.-14+900C>A
NM_001293180.2:c.-14+900C>A NP_001280109.1:n.-14+900C>A
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