Canonical Allele Identifier: CA5797967
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs770435368
ExAC: 11:1075628 C / G
gnomAD v2: 11-1075628-C-G
gnomAD v4: 11-1075628-C-G
MyVariant Identifiers: chr11:g.1075628C>G (hg19) chr11:g.1075628C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075628C>G , CM000673.2:g.1075628C>G GRCh38
NC_000011.9:g.1075628C>G , CM000673.1:g.1075628C>G GRCh37
NC_000011.8:g.1065628C>G NCBI36
NG_051929.1:g.5754C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-23C>G
ENST00000675028.1:c.77-23C>G ENSP00000502432.1:n.77-23C>G
NM_002457.3:c.77-23C>G NP_002448.3:n.77-23C>G
NM_002457.4:c.77-23C>G NP_002448.4:n.77-23C>G
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