Canonical Allele Identifier: CA472384522
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1093858A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099950A>T , CM000673.2:g.1099950A>T GRCh38
NC_000011.9:g.1093858A>T , CM000673.1:g.1093858A>T GRCh37
NC_000011.8:g.1083858A>T NCBI36
NG_051929.1:g.31977A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.9734A>T
ENST00000674892.1:c.181A>T ENSP00000501871.1:p.Thr61Ser
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