Canonical Allele Identifier: CA675557564
Gene: RCN1 HGNC NCBI
PAX6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1301213321
gnomAD v3: 11-31863310-C-A
gnomAD v4: 11-31863310-C-A
MyVariant Identifiers: chr11:g.31884856C>A (hg19) chr11:g.31863310C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.31863310C>A , CM000673.2:g.31863310C>A GRCh38
NC_000011.9:g.31884856C>A , CM000673.1:g.31884856C>A GRCh37
NC_000011.8:g.31841432C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000506388.2:n.75-21984C>A (RCN1)
ENST00000530348.5:c.-245+50813C>A (RCN1) ENSP00000436482.1:n.-245+50813C>A
ENST00000532942.5:c.101+46671C>A (RCN1) ENSP00000436422.1:n.101+46671C>A
NR_033971.1:n.75-21984C>A (PAX6-AS1)
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