Canonical Allele Identifier: CA671414332
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs10794288
MyVariant Identifiers: chr11:g.1086825C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1086825C>G , CM000673.2:g.1086825C>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.2643C>G
ENST00000675028.1:c.2616C>G ENSP00000502432.1:p.Asp872Glu
NM_002457.3:c.2616C>G NP_002448.3:p.Asp872Glu
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