Canonical Allele Identifier: CA472358449
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs2133874476
MyVariant Identifiers: chr11:g.1075698A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075698A>G , CM000673.2:g.1075698A>G GRCh38
NC_000011.9:g.1075698A>G , CM000673.1:g.1075698A>G GRCh37
NC_000011.8:g.1065698A>G NCBI36
NG_051929.1:g.5824A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.151A>G
ENST00000675028.1:c.124A>G ENSP00000502432.1:p.Asn42Asp
NM_002457.3:c.124A>G NP_002448.3:p.Asn42Asp
NM_002457.4:c.124A>G NP_002448.4:p.Asn42Asp
Search 100 bp 5'
Search 100 bp 3'