Canonical Allele Identifier: CA472358757
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075729T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075729T>C , CM000673.2:g.1075729T>C GRCh38
NC_000011.9:g.1075729T>C , CM000673.1:g.1075729T>C GRCh37
NC_000011.8:g.1065729T>C NCBI36
NG_051929.1:g.5855T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.182T>C
ENST00000675028.1:c.155T>C ENSP00000502432.1:p.Val52Ala
NM_002457.3:c.155T>C NP_002448.3:p.Val52Ala
NM_002457.4:c.155T>C NP_002448.4:p.Val52Ala
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