Canonical Allele Identifier: CA472384228
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1093760A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099852A>C , CM000673.2:g.1099852A>C GRCh38
NC_000011.9:g.1093760A>C , CM000673.1:g.1093760A>C GRCh37
NC_000011.8:g.1083760A>C NCBI36
NG_051929.1:g.31879A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9636A>C
ENST00000674892.1:c.83A>C ENSP00000501871.1:p.Gln28Pro
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