Canonical Allele Identifier: CA220285942
Gene: RCN1 HGNC NCBI
PAX6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs963906476
MyVariant Identifiers: chr11:g.31884790G>C (hg19) chr11:g.31863244G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.31863244G>C , CM000673.2:g.31863244G>C GRCh38
NC_000011.9:g.31884790G>C , CM000673.1:g.31884790G>C GRCh37
NC_000011.8:g.31841366G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506388.2:n.75-22050G>C (RCN1)
ENST00000530348.5:c.-245+50747G>C (RCN1) ENSP00000436482.1:n.-245+50747G>C
ENST00000532942.5:c.101+46605G>C (RCN1) ENSP00000436422.1:n.101+46605G>C
NR_033971.1:n.75-22050G>C (PAX6-AS1)
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