Canonical Allele Identifier: CA1947457101
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs1857870021
gnomAD v4: 11-1075635-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075635C>A , CM000673.2:g.1075635C>A GRCh38
NC_000011.9:g.1075635C>A , CM000673.1:g.1075635C>A GRCh37
NC_000011.8:g.1065635C>A NCBI36
NG_051929.1:g.5761C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-16C>A
ENST00000675028.1:c.77-16C>A ENSP00000502432.1:n.77-16C>A
NM_002457.3:c.77-16C>A NP_002448.3:n.77-16C>A
NM_002457.4:c.77-16C>A NP_002448.4:n.77-16C>A
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