Canonical Allele Identifier: CA472384255
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1093770G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099862G>C , CM000673.2:g.1099862G>C GRCh38
NC_000011.9:g.1093770G>C , CM000673.1:g.1093770G>C GRCh37
NC_000011.8:g.1083770G>C NCBI36
NG_051929.1:g.31889G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.9646G>C
ENST00000674892.1:c.93G>C ENSP00000501871.1:p.Arg31=