Canonical Allele Identifier: CA472384505
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs757797699
MyVariant Identifiers: chr11:g.1093853C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099945C>A , CM000673.2:g.1099945C>A GRCh38
NC_000011.9:g.1093853C>A , CM000673.1:g.1093853C>A GRCh37
NC_000011.8:g.1083853C>A NCBI36
NG_051929.1:g.31972C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9729C>A
ENST00000674892.1:c.176C>A ENSP00000501871.1:p.Pro59His