Canonical Allele Identifier: CA472358590
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075713A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075713A>C , CM000673.2:g.1075713A>C GRCh38
NC_000011.9:g.1075713A>C , CM000673.1:g.1075713A>C GRCh37
NC_000011.8:g.1065713A>C NCBI36
NG_051929.1:g.5839A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.166A>C
ENST00000675028.1:c.139A>C ENSP00000502432.1:p.Thr47Pro
NM_002457.3:c.139A>C NP_002448.3:p.Thr47Pro
NM_002457.4:c.139A>C NP_002448.4:p.Thr47Pro
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