Canonical Allele Identifier: CA472384490
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1093848C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099940C>T , CM000673.2:g.1099940C>T GRCh38
NC_000011.9:g.1093848C>T , CM000673.1:g.1093848C>T GRCh37
NC_000011.8:g.1083848C>T NCBI36
NG_051929.1:g.31967C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9724C>T
ENST00000674892.1:c.171C>T ENSP00000501871.1:p.Ala57=