Canonical Allele Identifier: CA472384502
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1172018945
gnomAD v2: 11-1093852-C-G
gnomAD v4: 11-1099944-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099944C>G , CM000673.2:g.1099944C>G GRCh38
NC_000011.9:g.1093852C>G , CM000673.1:g.1093852C>G GRCh37
NC_000011.8:g.1083852C>G NCBI36
NG_051929.1:g.31971C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9728C>G
ENST00000674892.1:c.175C>G ENSP00000501871.1:p.Pro59Ala