Canonical Allele Identifier: CA472384532
Gene: MUC2 HGNC NCBI

Linked Data

gnomAD v4: 11-1099953-C-A
MyVariant Identifiers: chr11:g.1093861C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099953C>A , CM000673.2:g.1099953C>A GRCh38
NC_000011.9:g.1093861C>A , CM000673.1:g.1093861C>A GRCh37
NC_000011.8:g.1083861C>A NCBI36
NG_051929.1:g.31980C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9737C>A
ENST00000674892.1:c.184C>A ENSP00000501871.1:p.Pro62Thr
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