Canonical Allele Identifier: CA472384520
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1093857C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099949C>G , CM000673.2:g.1099949C>G GRCh38
NC_000011.9:g.1093857C>G , CM000673.1:g.1093857C>G GRCh37
NC_000011.8:g.1083857C>G NCBI36
NG_051929.1:g.31976C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9733C>G
ENST00000674892.1:c.180C>G ENSP00000501871.1:p.Ser60=