Canonical Allele Identifier: CA472358215
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075673C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075673C>G , CM000673.2:g.1075673C>G GRCh38
NC_000011.9:g.1075673C>G , CM000673.1:g.1075673C>G GRCh37
NC_000011.8:g.1065673C>G NCBI36
NG_051929.1:g.5799C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.126C>G
ENST00000675028.1:c.99C>G ENSP00000502432.1:p.Gly33=
NM_002457.3:c.99C>G NP_002448.3:p.Gly33=
NM_002457.4:c.99C>G NP_002448.4:p.Gly33=
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