Canonical Allele Identifier: CA472392794
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1101087C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1107179C>G , CM000673.2:g.1107179C>G GRCh38
NC_000011.9:g.1101087C>G , CM000673.1:g.1101087C>G GRCh37
NC_000011.8:g.1091087C>G NCBI36
NG_051929.1:g.39202C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.11543C>G
ENST00000674892.1:c.1990C>G ENSP00000501871.1:p.Pro664Ala
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