Canonical Allele Identifier: CA1988804368

Linked Data

dbSNP Id: rs1949259396

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86948174G>A , CM000673.2:g.86948174G>A GRCh38
NC_000011.9:g.86659216G>A , CM000673.1:g.86659216G>A GRCh37
NC_000011.8:g.86336864G>A NCBI36
NG_011752.1:g.12218C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.*2968C>T (FZD4) MANE Select ENSP00000434034.1:n.*2968C>T
ENST00000528769.5:n.129-2182G>A (PRSS23)
ENST00000531380.1:c.*2968C>T (FZD4) ENSP00000434034.1:n.*2968C>T
ENST00000531521.1:n.243-2182G>A (PRSS23)
ENST00000532234.5:c.*65-2182G>A (PRSS23) ENSP00000436676.1:n.*65-2182G>A
ENST00000533902.2:c.207-3042G>A (PRSS23) ENSP00000437268.1:n.207-3042G>A
NM_012193.3:c.*2968C>T (FZD4) NP_036325.2:n.*2968C>T
NR_120591.1:n.737-2182G>A (PRSS23)
NR_120592.1:n.630-3042G>A (PRSS23)
NR_120591.2:n.435-2182G>A (PRSS23)
NR_120592.2:n.328-3042G>A (PRSS23)
NM_012193.4:c.*2968C>T (FZD4) MANE Select NP_036325.2:n.*2968C>T
NR_120591.3:n.435-2182G>A (PRSS23)