Canonical Allele Identifier: CA472358620
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075716T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075716T>A , CM000673.2:g.1075716T>A GRCh38
NC_000011.9:g.1075716T>A , CM000673.1:g.1075716T>A GRCh37
NC_000011.8:g.1065716T>A NCBI36
NG_051929.1:g.5842T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.169T>A
ENST00000675028.1:c.142T>A ENSP00000502432.1:p.Phe48Ile
NM_002457.3:c.142T>A NP_002448.3:p.Phe48Ile
NM_002457.4:c.142T>A NP_002448.4:p.Phe48Ile
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