Canonical Allele Identifier: CA472358219
Gene: MUC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.1075674C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075674C>A , CM000673.2:g.1075674C>A GRCh38
NC_000011.9:g.1075674C>A , CM000673.1:g.1075674C>A GRCh37
NC_000011.8:g.1065674C>A NCBI36
NG_051929.1:g.5800C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.127C>A
ENST00000675028.1:c.100C>A ENSP00000502432.1:p.His34Asn
NM_002457.3:c.100C>A NP_002448.3:p.His34Asn
NM_002457.4:c.100C>A NP_002448.4:p.His34Asn