Canonical Allele Identifier: CA217001183
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1000072343
gnomAD v4: 11-1099952-A-T
MyVariant Identifiers: chr11:g.1093860A>T (hg19) chr11:g.1099952A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099952A>T , CM000673.2:g.1099952A>T GRCh38
NC_000011.9:g.1093860A>T , CM000673.1:g.1093860A>T GRCh37
NC_000011.8:g.1083860A>T NCBI36
NG_051929.1:g.31979A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.9736A>T
ENST00000674892.1:c.183A>T ENSP00000501871.1:p.Thr61=
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