Canonical Allele Identifier: CA220285960
Gene: RCN1 HGNC NCBI
PAX6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs944308138

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.31863457A>C , CM000673.2:g.31863457A>C GRCh38
NC_000011.9:g.31885003A>C , CM000673.1:g.31885003A>C GRCh37
NC_000011.8:g.31841579A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000506388.2:n.75-21837A>C (RCN1)
ENST00000530348.5:c.-245+50960A>C (RCN1) ENSP00000436482.1:n.-245+50960A>C
ENST00000532942.5:c.101+46818A>C (RCN1) ENSP00000436422.1:n.101+46818A>C
NR_033971.1:n.75-21837A>C (PAX6-AS1)