Canonical Allele Identifier: CA5800471
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs748088911
gnomAD v2: 11-1093851-A-C
gnomAD v4: 11-1099943-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099943A>C , CM000673.2:g.1099943A>C GRCh38
NC_000011.9:g.1093851A>C , CM000673.1:g.1093851A>C GRCh37
NC_000011.8:g.1083851A>C NCBI36
NG_051929.1:g.31970A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9727A>C
ENST00000674892.1:c.174A>C ENSP00000501871.1:p.Pro58=