Canonical Allele Identifier: CA472359010
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075758A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075758A>G , CM000673.2:g.1075758A>G GRCh38
NC_000011.9:g.1075758A>G , CM000673.1:g.1075758A>G GRCh37
NC_000011.8:g.1065758A>G NCBI36
NG_051929.1:g.5884A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.211A>G
ENST00000675028.1:c.184A>G ENSP00000502432.1:p.Asn62Asp
NM_002457.3:c.184A>G NP_002448.3:p.Asn62Asp
NM_002457.4:c.184A>G NP_002448.4:p.Asn62Asp
Search 100 bp 5'
Search 100 bp 3'