Canonical Allele Identifier: CA472358777
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075731T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075731T>C , CM000673.2:g.1075731T>C GRCh38
NC_000011.9:g.1075731T>C , CM000673.1:g.1075731T>C GRCh37
NC_000011.8:g.1065731T>C NCBI36
NG_051929.1:g.5857T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.184T>C
ENST00000675028.1:c.157T>C ENSP00000502432.1:p.Phe53Leu
NM_002457.3:c.157T>C NP_002448.3:p.Phe53Leu
NM_002457.4:c.157T>C NP_002448.4:p.Phe53Leu
Search 100 bp 5'
Search 100 bp 3'