Canonical Allele Identifier: CA472392538
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1100999G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1107091G>A , CM000673.2:g.1107091G>A GRCh38
NC_000011.9:g.1100999G>A , CM000673.1:g.1100999G>A GRCh37
NC_000011.8:g.1090999G>A NCBI36
NG_051929.1:g.39114G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.11455G>A
ENST00000674892.1:c.1902G>A ENSP00000501871.1:p.Gly634=
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