Canonical Allele Identifier: CA217001018
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs936776345
gnomAD v3: 11-1099846-C-G
gnomAD v4: 11-1099846-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099846C>G , CM000673.2:g.1099846C>G GRCh38
NC_000011.9:g.1093754C>G , CM000673.1:g.1093754C>G GRCh37
NC_000011.8:g.1083754C>G NCBI36
NG_051929.1:g.31873C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.9630C>G
ENST00000674892.1:c.77C>G ENSP00000501871.1:p.Thr26Ser