Canonical Allele Identifier: CA5800425
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs753252386
ExAC: 11:1093764 C / A
gnomAD v2: 11-1093764-C-A
gnomAD v4: 11-1099856-C-A
MyVariant Identifiers: chr11:g.1093764C>A (hg19) chr11:g.1099856C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099856C>A , CM000673.2:g.1099856C>A GRCh38
NC_000011.9:g.1093764C>A , CM000673.1:g.1093764C>A GRCh37
NC_000011.8:g.1083764C>A NCBI36
NG_051929.1:g.31883C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9640C>A
ENST00000674892.1:c.87C>A ENSP00000501871.1:p.Thr29=
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