Canonical Allele Identifier: CA5801190
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs762727837
ExAC: 11:1100981 T / A
gnomAD v2: 11-1100981-T-A
gnomAD v3: 11-1107073-T-A
gnomAD v4: 11-1107073-T-A
MyVariant Identifiers: chr11:g.1100981T>A (hg19) chr11:g.1107073T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1107073T>A , CM000673.2:g.1107073T>A GRCh38
NC_000011.9:g.1100981T>A , CM000673.1:g.1100981T>A GRCh37
NC_000011.8:g.1090981T>A NCBI36
NG_051929.1:g.39096T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.11450-13T>A
ENST00000674892.1:c.1897-13T>A ENSP00000501871.1:n.1897-13T>A
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