Canonical Allele Identifier: CA225379921

Linked Data

dbSNP Id: rs3740662

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950901T>C , CM000673.2:g.86950901T>C GRCh38
NC_000011.9:g.86661943T>C , CM000673.1:g.86661943T>C GRCh37
NC_000011.8:g.86339591T>C NCBI36
NG_011752.1:g.9491A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*241A>G (FZD4) MANE Select ENSP00000434034.1:n.*241A>G
ENST00000528769.5:n.273-315T>C (PRSS23)
ENST00000531380.1:c.*241A>G (FZD4) ENSP00000434034.1:n.*241A>G
ENST00000531521.1:n.387-315T>C (PRSS23)
ENST00000532234.5:c.*209-315T>C (PRSS23) ENSP00000436676.1:n.*209-315T>C
ENST00000533902.2:c.207-315T>C (PRSS23) ENSP00000437268.1:n.207-315T>C
NM_012193.3:c.*241A>G (FZD4) NP_036325.2:n.*241A>G
NR_120591.1:n.881-315T>C (PRSS23)
NR_120592.1:n.630-315T>C (PRSS23)
NR_120591.2:n.579-315T>C (PRSS23)
NR_120592.2:n.328-315T>C (PRSS23)
NM_012193.4:c.*241A>G (FZD4) MANE Select NP_036325.2:n.*241A>G
NR_120591.3:n.579-315T>C (PRSS23)