Canonical Allele Identifier: CA476144611

Linked Data

dbSNP Id: rs1251905596

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952045T>G , CM000673.2:g.86952045T>G GRCh38
NC_000011.9:g.86663087T>G , CM000673.1:g.86663087T>G GRCh37
NC_000011.8:g.86340735T>G NCBI36
NG_011752.1:g.8347A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.711A>C (FZD4) MANE Select ENSP00000434034.1:p.Thr237=
ENST00000531380.1:c.711A>C (FZD4) ENSP00000434034.1:p.Thr237=
ENST00000532234.5:c.*1038T>G (PRSS23) ENSP00000436676.1:n.*1038T>G
ENST00000533902.2:c.*760T>G (PRSS23) ENSP00000437268.1:n.*760T>G
NM_012193.3:c.711A>C (FZD4) NP_036325.2:p.Thr237=
NR_120591.1:n.1710T>G (PRSS23)
NR_120592.1:n.1459T>G (PRSS23)
NR_120591.2:n.1408T>G (PRSS23)
NR_120592.2:n.1157T>G (PRSS23)
NM_012193.4:c.711A>C (FZD4) MANE Select NP_036325.2:p.Thr237=
NR_120591.3:n.1408T>G (PRSS23)