Canonical Allele Identifier: CA472358632
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075717T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075717T>C , CM000673.2:g.1075717T>C GRCh38
NC_000011.9:g.1075717T>C , CM000673.1:g.1075717T>C GRCh37
NC_000011.8:g.1065717T>C NCBI36
NG_051929.1:g.5843T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.170T>C
ENST00000675028.1:c.143T>C ENSP00000502432.1:p.Phe48Ser
NM_002457.3:c.143T>C NP_002448.3:p.Phe48Ser
NM_002457.4:c.143T>C NP_002448.4:p.Phe48Ser