Canonical Allele Identifier: CA6218285

Linked Data

dbSNP Id: rs772349259

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951146A>C , CM000673.2:g.86951146A>C GRCh38
NC_000011.9:g.86662188A>C , CM000673.1:g.86662188A>C GRCh37
NC_000011.8:g.86339836A>C NCBI36
NG_011752.1:g.9246T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1610T>G (FZD4) MANE Select ENSP00000434034.1:p.Val537Gly
ENST00000528769.5:n.273-70A>C (PRSS23)
ENST00000531380.1:c.1610T>G (FZD4) ENSP00000434034.1:p.Val537Gly
ENST00000531521.1:n.387-70A>C (PRSS23)
ENST00000532234.5:c.*209-70A>C (PRSS23) ENSP00000436676.1:n.*209-70A>C
ENST00000533902.2:c.207-70A>C (PRSS23) ENSP00000437268.1:n.207-70A>C
NM_012193.3:c.1610T>G (FZD4) NP_036325.2:p.Val537Gly
NR_120591.1:n.881-70A>C (PRSS23)
NR_120592.1:n.630-70A>C (PRSS23)
NR_120591.2:n.579-70A>C (PRSS23)
NR_120592.2:n.328-70A>C (PRSS23)
NM_012193.4:c.1610T>G (FZD4) MANE Select NP_036325.2:p.Val537Gly
NR_120591.3:n.579-70A>C (PRSS23)