Canonical Allele Identifier: CA5800429
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs531918496
gnomAD v2: 11-1093768-C-T
gnomAD v3: 11-1099860-C-T
gnomAD v4: 11-1099860-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099860C>T , CM000673.2:g.1099860C>T GRCh38
NC_000011.9:g.1093768C>T , CM000673.1:g.1093768C>T GRCh37
NC_000011.8:g.1083768C>T NCBI36
NG_051929.1:g.31887C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9644C>T
ENST00000674892.1:c.91C>T ENSP00000501871.1:p.Arg31Trp