Canonical Allele Identifier: CA472384484
Gene: MUC2 HGNC NCBI

Linked Data

gnomAD v4: 11-1099938-G-T
MyVariant Identifiers: chr11:g.1093846G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099938G>T , CM000673.2:g.1099938G>T GRCh38
NC_000011.9:g.1093846G>T , CM000673.1:g.1093846G>T GRCh37
NC_000011.8:g.1083846G>T NCBI36
NG_051929.1:g.31965G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9722G>T
ENST00000674892.1:c.169G>T ENSP00000501871.1:p.Ala57Ser