Canonical Allele Identifier: CA472384227
Gene: MUC2 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9636A>T
ENST00000674892.1:c.83A>T ENSP00000501871.1:p.Gln28Leu
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