Canonical Allele Identifier: CA472392802
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1101091T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1107183T>A , CM000673.2:g.1107183T>A GRCh38
NC_000011.9:g.1101091T>A , CM000673.1:g.1101091T>A GRCh37
NC_000011.8:g.1091091T>A NCBI36
NG_051929.1:g.39206T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.11547T>A
ENST00000674892.1:c.1994T>A ENSP00000501871.1:p.Val665Asp
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