Canonical Allele Identifier: CA5797966
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs756337347
ExAC: 11:1075625 C / CCGCTGCT
gnomAD v2: 11-1075625-C-CCGCTGCT
gnomAD v3: 11-1075625-C-CCGCTGCT
gnomAD v4: 11-1075625-C-CCGCTGCT
MyVariant Identifiers: chr11:g.1075625_1075626insCGCTGCT (hg19) chr11:g.1075625_1075626insCGCTGCT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075626_1075627insGCTGCTC , CM000673.2:g.1075626_1075627insGCTGCTC GRCh38
NC_000011.9:g.1075626_1075627insGCTGCTC , CM000673.1:g.1075626_1075627insGCTGCTC GRCh37
NC_000011.8:g.1065626_1065627insGCTGCTC NCBI36
NG_051929.1:g.5752_5753insGCTGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-25_104-24insGCTGCTC
ENST00000675028.1:c.77-25_77-24insGCTGCTC ENSP00000502432.1:n.77-25_77-24insGCTGCTC
NM_002457.3:c.77-25_77-24insGCTGCTC NP_002448.3:n.77-25_77-24insGCTGCTC
NM_002457.4:c.77-25_77-24insGCTGCTC NP_002448.4:n.77-25_77-24insGCTGCTC
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