Canonical Allele Identifier: CA5797986
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs745502643
ExAC: 11:1075697 C / A
gnomAD v2: 11-1075697-C-A
gnomAD v3: 11-1075697-C-A
gnomAD v4: 11-1075697-C-A
MyVariant Identifiers: chr11:g.1075697C>A (hg19) chr11:g.1075697C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075697C>A , CM000673.2:g.1075697C>A GRCh38
NC_000011.9:g.1075697C>A , CM000673.1:g.1075697C>A GRCh37
NC_000011.8:g.1065697C>A NCBI36
NG_051929.1:g.5823C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.150C>A
ENST00000675028.1:c.123C>A ENSP00000502432.1:p.Gly41=
NM_002457.3:c.123C>A NP_002448.3:p.Gly41=
NM_002457.4:c.123C>A NP_002448.4:p.Gly41=
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