Canonical Allele Identifier: CA472384241
Gene: MUC2 HGNC NCBI

Linked Data

gnomAD v4: 11-1099857-T-G
MyVariant Identifiers: chr11:g.1093765T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099857T>G , CM000673.2:g.1099857T>G GRCh38
NC_000011.9:g.1093765T>G , CM000673.1:g.1093765T>G GRCh37
NC_000011.8:g.1083765T>G NCBI36
NG_051929.1:g.31884T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.9641T>G
ENST00000674892.1:c.88T>G ENSP00000501871.1:p.Ser30Ala