Canonical Allele Identifier: CA472358150
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075667C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075667C>G , CM000673.2:g.1075667C>G GRCh38
NC_000011.9:g.1075667C>G , CM000673.1:g.1075667C>G GRCh37
NC_000011.8:g.1065667C>G NCBI36
NG_051929.1:g.5793C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.120C>G
ENST00000675028.1:c.93C>G ENSP00000502432.1:p.Asn31Lys
NM_002457.3:c.93C>G NP_002448.3:p.Asn31Lys
NM_002457.4:c.93C>G NP_002448.4:p.Asn31Lys
Search 100 bp 5'
Search 100 bp 3'