Canonical Allele Identifier: CA220285958
Gene: RCN1 HGNC NCBI
PAX6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs780583338

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.31863405A>G , CM000673.2:g.31863405A>G GRCh38
NC_000011.9:g.31884951A>G , CM000673.1:g.31884951A>G GRCh37
NC_000011.8:g.31841527A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000506388.2:n.75-21889A>G (RCN1)
ENST00000530348.5:c.-245+50908A>G (RCN1) ENSP00000436482.1:n.-245+50908A>G
ENST00000532942.5:c.101+46766A>G (RCN1) ENSP00000436422.1:n.101+46766A>G
NR_033971.1:n.75-21889A>G (PAX6-AS1)