Canonical Allele Identifier: CA5797957
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs756393406
ExAC: 11:1075601 G / A
gnomAD v2: 11-1075601-G-A
gnomAD v4: 11-1075601-G-A
MyVariant Identifiers: chr11:g.1075601G>A (hg19) chr11:g.1075601G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075601G>A , CM000673.2:g.1075601G>A GRCh38
NC_000011.9:g.1075601G>A , CM000673.1:g.1075601G>A GRCh37
NC_000011.8:g.1065601G>A NCBI36
NG_051929.1:g.5727G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-50G>A
ENST00000675028.1:c.77-50G>A ENSP00000502432.1:n.77-50G>A
NM_002457.3:c.77-50G>A NP_002448.3:n.77-50G>A
NM_002457.4:c.77-50G>A NP_002448.4:n.77-50G>A
Search 100 bp 5'
Search 100 bp 3'