Canonical Allele Identifier: CA472384245
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1093766C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099858C>A , CM000673.2:g.1099858C>A GRCh38
NC_000011.9:g.1093766C>A , CM000673.1:g.1093766C>A GRCh37
NC_000011.8:g.1083766C>A NCBI36
NG_051929.1:g.31885C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.9642C>A
ENST00000674892.1:c.89C>A ENSP00000501871.1:p.Ser30Tyr