Canonical Allele Identifier: CA3055379

Gene: PRSS12

Linked Data

• ClinVar Variation Id: 436424
• ClinVar RCV Id: RCV000504125 ; RCV000918544
• dbSNP Id: rs199574216
• ExAC: 4:119203343 C / T
• gnomAD v2: 4-119203343-C-T
• gnomAD v3: 4-118282188-C-T
• gnomAD v4: 4-118282188-C-T
• MyVariant Identifiers: chr4:g.119203343C>T (hg19) ; chr4:g.118282188C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118282188C>T , CM000666.2:g.118282188C>T	GRCh38
NC_000004.11:g.119203343C>T , CM000666.1:g.119203343C>T	GRCh37
NC_000004.10:g.119422791C>T	NCBI36
NG_023350.1:g.75580G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296498.3:c.2376G>A MANE Select	ENSP00000296498.3:p.Arg792=
NM_003619.3:c.2376G>A	NP_003610.2:p.Arg792=
NM_003619.4:c.2376G>A MANE Select	NP_003610.2:p.Arg792=