Canonical Allele Identifier: CA472358386
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075692T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075692T>G , CM000673.2:g.1075692T>G GRCh38
NC_000011.9:g.1075692T>G , CM000673.1:g.1075692T>G GRCh37
NC_000011.8:g.1065692T>G NCBI36
NG_051929.1:g.5818T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.145T>G
ENST00000675028.1:c.118T>G ENSP00000502432.1:p.Trp40Gly
NM_002457.3:c.118T>G NP_002448.3:p.Trp40Gly
NM_002457.4:c.118T>G NP_002448.4:p.Trp40Gly