Canonical Allele Identifier: CA1947471169
Gene: MUC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099955C= , CM000673.2:g.1099955C= GRCh38
NC_000011.9:g.1093863C= , CM000673.1:g.1093863C= GRCh37
NC_000011.8:g.1083863C= NCBI36
NG_051929.1:g.31982C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.9739C=
ENST00000674892.1:c.186C= ENSP00000501871.1:p.Pro62=