Canonical Allele Identifier: CA216976698
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs2856097
MyVariant Identifiers: chr11:g.1075675A>G (hg19) chr11:g.1075675A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075675A>G , CM000673.2:g.1075675A>G GRCh38
NC_000011.9:g.1075675A>G , CM000673.1:g.1075675A>G GRCh37
NC_000011.8:g.1065675A>G NCBI36
NG_051929.1:g.5801A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.128A>G
ENST00000675028.1:c.101A>G ENSP00000502432.1:p.His34Arg
NM_002457.3:c.101A>G NP_002448.3:p.His34Arg
NM_002457.4:c.101A>G NP_002448.4:p.His34Arg
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