Canonical Allele Identifier: CA472358004
Gene: MUC2 HGNC NCBI

Linked Data

gnomAD v4: 11-1075654-G-A
MyVariant Identifiers: chr11:g.1075654G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075654G>A , CM000673.2:g.1075654G>A GRCh38
NC_000011.9:g.1075654G>A , CM000673.1:g.1075654G>A GRCh37
NC_000011.8:g.1065654G>A NCBI36
NG_051929.1:g.5780G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.107G>A
ENST00000675028.1:c.80G>A ENSP00000502432.1:p.Gly27Asp
NM_002457.3:c.80G>A NP_002448.3:p.Gly27Asp
NM_002457.4:c.80G>A NP_002448.4:p.Gly27Asp
Search 100 bp 5'
Search 100 bp 3'