Canonical Allele Identifier: CA472359101
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075768C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075768C>A , CM000673.2:g.1075768C>A GRCh38
NC_000011.9:g.1075768C>A , CM000673.1:g.1075768C>A GRCh37
NC_000011.8:g.1065768C>A NCBI36
NG_051929.1:g.5894C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.221C>A
ENST00000675028.1:c.194C>A ENSP00000502432.1:p.Ser65Tyr
NM_002457.3:c.194C>A NP_002448.3:p.Ser65Tyr
NM_002457.4:c.194C>A NP_002448.4:p.Ser65Tyr
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