Canonical Allele Identifier: CA5800470
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs754897881
gnomAD v2: 11-1093850-C-A
gnomAD v4: 11-1099942-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099942C>A , CM000673.2:g.1099942C>A GRCh38
NC_000011.9:g.1093850C>A , CM000673.1:g.1093850C>A GRCh37
NC_000011.8:g.1083850C>A NCBI36
NG_051929.1:g.31969C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9726C>A
ENST00000674892.1:c.173C>A ENSP00000501871.1:p.Pro58Gln