Canonical Allele Identifier: CA1947471150
Gene: MUC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099951C= , CM000673.2:g.1099951C= GRCh38
NC_000011.9:g.1093859C= , CM000673.1:g.1093859C= GRCh37
NC_000011.8:g.1083859C= NCBI36
NG_051929.1:g.31978C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.9735C=
ENST00000674892.1:c.182C= ENSP00000501871.1:p.Thr61=