Canonical Allele Identifier: CA598375466
Gene: RCN1 HGNC NCBI
PAX6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1308129623

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.31863368C>T , CM000673.2:g.31863368C>T GRCh38
NC_000011.9:g.31884914C>T , CM000673.1:g.31884914C>T GRCh37
NC_000011.8:g.31841490C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506388.2:n.75-21926C>T (RCN1)
ENST00000530348.5:c.-245+50871C>T (RCN1) ENSP00000436482.1:n.-245+50871C>T
ENST00000532942.5:c.101+46729C>T (RCN1) ENSP00000436422.1:n.101+46729C>T
NR_033971.1:n.75-21926C>T (PAX6-AS1)