Canonical Allele Identifier: CA5800474
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs746607278
gnomAD v2: 11-1093856-C-A
gnomAD v4: 11-1099948-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099948C>A , CM000673.2:g.1099948C>A GRCh38
NC_000011.9:g.1093856C>A , CM000673.1:g.1093856C>A GRCh37
NC_000011.8:g.1083856C>A NCBI36
NG_051929.1:g.31975C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9732C>A
ENST00000674892.1:c.179C>A ENSP00000501871.1:p.Ser60Tyr