Canonical Allele Identifier: CA216976578
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs926169154
MyVariant Identifiers: chr11:g.1075616G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075616G>A , CM000673.2:g.1075616G>A GRCh38
NC_000011.9:g.1075616G>A , CM000673.1:g.1075616G>A GRCh37
NC_000011.8:g.1065616G>A NCBI36
NG_051929.1:g.5742G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-35G>A
ENST00000675028.1:c.77-35G>A ENSP00000502432.1:n.77-35G>A
NM_002457.3:c.77-35G>A NP_002448.3:n.77-35G>A
NM_002457.4:c.77-35G>A NP_002448.4:n.77-35G>A
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