Canonical Allele Identifier: CA472384254
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs41361144
gnomAD v2: 11-1093769-G-T
gnomAD v4: 11-1099861-G-T
MyVariant Identifiers: chr11:g.1093769G>T (hg19) chr11:g.1099861G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099861G>T , CM000673.2:g.1099861G>T GRCh38
NC_000011.9:g.1093769G>T , CM000673.1:g.1093769G>T GRCh37
NC_000011.8:g.1083769G>T NCBI36
NG_051929.1:g.31888G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9645G>T
ENST00000674892.1:c.92G>T ENSP00000501871.1:p.Arg31Leu
Search 100 bp 5'
Search 100 bp 3'