Canonical Allele Identifier: CA472384513
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1093855T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099947T>G , CM000673.2:g.1099947T>G GRCh38
NC_000011.9:g.1093855T>G , CM000673.1:g.1093855T>G GRCh37
NC_000011.8:g.1083855T>G NCBI36
NG_051929.1:g.31974T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9731T>G
ENST00000674892.1:c.178T>G ENSP00000501871.1:p.Ser60Ala