Canonical Allele Identifier: CA5800432
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs769769719
ExAC: 11:1093770 G / A
gnomAD v2: 11-1093770-G-A
gnomAD v4: 11-1099862-G-A
MyVariant Identifiers: chr11:g.1093770G>A (hg19) chr11:g.1099862G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099862G>A , CM000673.2:g.1099862G>A GRCh38
NC_000011.9:g.1093770G>A , CM000673.1:g.1093770G>A GRCh37
NC_000011.8:g.1083770G>A NCBI36
NG_051929.1:g.31889G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9646G>A
ENST00000674892.1:c.93G>A ENSP00000501871.1:p.Arg31=
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