Canonical Allele Identifier: CA216976558
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs917353786
MyVariant Identifiers: chr11:g.1075606C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075606C>A , CM000673.2:g.1075606C>A GRCh38
NC_000011.9:g.1075606C>A , CM000673.1:g.1075606C>A GRCh37
NC_000011.8:g.1065606C>A NCBI36
NG_051929.1:g.5732C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-45C>A
ENST00000675028.1:c.77-45C>A ENSP00000502432.1:n.77-45C>A
NM_002457.3:c.77-45C>A NP_002448.3:n.77-45C>A
NM_002457.4:c.77-45C>A NP_002448.4:n.77-45C>A
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