Canonical Allele Identifier: CA472358524
Gene: MUC2 HGNC NCBI

Linked Data

gnomAD v4: 11-1075706-C-A
MyVariant Identifiers: chr11:g.1075706C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075706C>A , CM000673.2:g.1075706C>A GRCh38
NC_000011.9:g.1075706C>A , CM000673.1:g.1075706C>A GRCh37
NC_000011.8:g.1065706C>A NCBI36
NG_051929.1:g.5832C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.159C>A
ENST00000675028.1:c.132C>A ENSP00000502432.1:p.His44Gln
NM_002457.3:c.132C>A NP_002448.3:p.His44Gln
NM_002457.4:c.132C>A NP_002448.4:p.His44Gln