Canonical Allele Identifier: CA472384500
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1093851A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099943A>G , CM000673.2:g.1099943A>G GRCh38
NC_000011.9:g.1093851A>G , CM000673.1:g.1093851A>G GRCh37
NC_000011.8:g.1083851A>G NCBI36
NG_051929.1:g.31970A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9727A>G
ENST00000674892.1:c.174A>G ENSP00000501871.1:p.Pro58=