Canonical Allele Identifier: CA2611828832
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs2133874260
gnomAD v4: 11-1075504-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075504A>C , CM000673.2:g.1075504A>C GRCh38
NC_000011.9:g.1075504A>C , CM000673.1:g.1075504A>C GRCh37
NC_000011.8:g.1065504A>C NCBI36
NG_051929.1:g.5630A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-147A>C
ENST00000675028.1:c.77-147A>C ENSP00000502432.1:n.77-147A>C
NM_002457.3:c.77-147A>C NP_002448.3:n.77-147A>C
NM_002457.4:c.77-147A>C NP_002448.4:n.77-147A>C
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