Canonical Allele Identifier: CA472357990
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1320741680
gnomAD v2: 11-1075652-G-C
gnomAD v4: 11-1075652-G-C
MyVariant Identifiers: chr11:g.1075652G>C (hg19) chr11:g.1075652G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075652G>C , CM000673.2:g.1075652G>C GRCh38
NC_000011.9:g.1075652G>C , CM000673.1:g.1075652G>C GRCh37
NC_000011.8:g.1065652G>C NCBI36
NG_051929.1:g.5778G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.105G>C
ENST00000675028.1:c.78G>C ENSP00000502432.1:p.Glu26Asp
NM_002457.3:c.78G>C NP_002448.3:p.Glu26Asp
NM_002457.4:c.78G>C NP_002448.4:p.Glu26Asp
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