Canonical Allele Identifier: CA5800431
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs41361144
ExAC: 11:1093769 G / C
gnomAD v2: 11-1093769-G-C
gnomAD v4: 11-1099861-G-C
MyVariant Identifiers: chr11:g.1093769G>C (hg19) chr11:g.1099861G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099861G>C , CM000673.2:g.1099861G>C GRCh38
NC_000011.9:g.1093769G>C , CM000673.1:g.1093769G>C GRCh37
NC_000011.8:g.1083769G>C NCBI36
NG_051929.1:g.31888G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9645G>C
ENST00000674892.1:c.92G>C ENSP00000501871.1:p.Arg31Pro
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