Canonical Allele Identifier: CA472358729
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075726A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075726A>G , CM000673.2:g.1075726A>G GRCh38
NC_000011.9:g.1075726A>G , CM000673.1:g.1075726A>G GRCh37
NC_000011.8:g.1065726A>G NCBI36
NG_051929.1:g.5852A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.179A>G
ENST00000675028.1:c.152A>G ENSP00000502432.1:p.Asp51Gly
NM_002457.3:c.152A>G NP_002448.3:p.Asp51Gly
NM_002457.4:c.152A>G NP_002448.4:p.Asp51Gly
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