Canonical Allele Identifier: CA1947457052
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1590076850
gnomAD v3: 11-1075615-G-C
gnomAD v4: 11-1075615-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075615G>C , CM000673.2:g.1075615G>C GRCh38
NC_000011.9:g.1075615G>C , CM000673.1:g.1075615G>C GRCh37
NC_000011.8:g.1065615G>C NCBI36
NG_051929.1:g.5741G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-36G>C
ENST00000675028.1:c.77-36G>C ENSP00000502432.1:n.77-36G>C
NM_002457.3:c.77-36G>C NP_002448.3:n.77-36G>C
NM_002457.4:c.77-36G>C NP_002448.4:n.77-36G>C
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