Canonical Allele Identifier: CA5797970
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs764497960
ExAC: 11:1075633 T / C
gnomAD v2: 11-1075633-T-C
gnomAD v3: 11-1075633-T-C
gnomAD v4: 11-1075633-T-C
MyVariant Identifiers: chr11:g.1075633T>C (hg19) chr11:g.1075633T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075633T>C , CM000673.2:g.1075633T>C GRCh38
NC_000011.9:g.1075633T>C , CM000673.1:g.1075633T>C GRCh37
NC_000011.8:g.1065633T>C NCBI36
NG_051929.1:g.5759T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-18T>C
ENST00000675028.1:c.77-18T>C ENSP00000502432.1:n.77-18T>C
NM_002457.3:c.77-18T>C NP_002448.3:n.77-18T>C
NM_002457.4:c.77-18T>C NP_002448.4:n.77-18T>C
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