Canonical Allele Identifier: CA472384248
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1312343769
gnomAD v3: 11-1099859-T-C
gnomAD v4: 11-1099859-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099859T>C , CM000673.2:g.1099859T>C GRCh38
NC_000011.9:g.1093767T>C , CM000673.1:g.1093767T>C GRCh37
NC_000011.8:g.1083767T>C NCBI36
NG_051929.1:g.31886T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.9643T>C
ENST00000674892.1:c.90T>C ENSP00000501871.1:p.Ser30=