Canonical Allele Identifier: CA216976659
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs756195200
gnomAD v2: 11-1075651-A-T
gnomAD v3: 11-1075651-A-T
gnomAD v4: 11-1075651-A-T
MyVariant Identifiers: chr11:g.1075651A>T (hg19) chr11:g.1075651A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075651A>T , CM000673.2:g.1075651A>T GRCh38
NC_000011.9:g.1075651A>T , CM000673.1:g.1075651A>T GRCh37
NC_000011.8:g.1065651A>T NCBI36
NG_051929.1:g.5777A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104A>T
ENST00000675028.1:c.77A>T ENSP00000502432.1:p.Glu26Val
NM_002457.3:c.77A>T NP_002448.3:p.Glu26Val
NM_002457.4:c.77A>T NP_002448.4:p.Glu26Val
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