Canonical Allele Identifier: CA216976741
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs148415065
MyVariant Identifiers: chr11:g.1075696_1075697insA (hg19) chr11:g.1075696_1075697insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075696_1075697insA , CM000673.2:g.1075696_1075697insA GRCh38
NC_000011.9:g.1075696_1075697insA , CM000673.1:g.1075696_1075697insA GRCh37
NC_000011.8:g.1065696_1065697insA NCBI36
NG_051929.1:g.5822_5823insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.149_150insA
ENST00000675028.1:c.122_123insA ENSP00000502432.1:p.Asn42GlnfsTer?
NM_002457.3:c.122_123insA NP_002448.3:p.Asn42GlnfsTer?
NM_002457.4:c.122_123insA NP_002448.4:p.Asn42GlnfsTer?
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