Canonical Allele Identifier: CA671342852
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1219877547
gnomAD v4: 11-1075529-G-T
MyVariant Identifiers: chr11:g.1075529G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075529G>T , CM000673.2:g.1075529G>T GRCh38
NC_000011.9:g.1075529G>T , CM000673.1:g.1075529G>T GRCh37
NC_000011.8:g.1065529G>T NCBI36
NG_051929.1:g.5655G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-122G>T
ENST00000675028.1:c.77-122G>T ENSP00000502432.1:n.77-122G>T
NM_002457.3:c.77-122G>T NP_002448.3:n.77-122G>T
NM_002457.4:c.77-122G>T NP_002448.4:n.77-122G>T
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