Canonical Allele Identifier: CA472358627
Gene: MUC2 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.169T>G
ENST00000675028.1:c.142T>G ENSP00000502432.1:p.Phe48Val
NM_002457.3:c.142T>G NP_002448.3:p.Phe48Val
NM_002457.4:c.142T>G NP_002448.4:p.Phe48Val
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