Canonical Allele Identifier: CA472358301
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075683T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075683T>A , CM000673.2:g.1075683T>A GRCh38
NC_000011.9:g.1075683T>A , CM000673.1:g.1075683T>A GRCh37
NC_000011.8:g.1065683T>A NCBI36
NG_051929.1:g.5809T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.136T>A
ENST00000675028.1:c.109T>A ENSP00000502432.1:p.Cys37Ser
NM_002457.3:c.109T>A NP_002448.3:p.Cys37Ser
NM_002457.4:c.109T>A NP_002448.4:p.Cys37Ser